Medicine
Ciprofloxacin 750 mg tablet
Ciprofloxacin 750 mg tablet is a generic prescription medicine for oral use, made by 14 labelers, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.
Availability
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
Store at 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59°…
Key facts
- Active ingredient (INN)
- Ciprofloxacin
- Brand
- Sold under the generic name
- Strength
- 750 mg
- Dosage form
- Tablet
- Route
- Oral
- Packs
- 50 tablets, 100 tablets, 500 tablets and 46 more
- Manufacturers
- Aurobindo PharmaIndiaBryant Ranch PrepackHawaii RepackChartwell RXAmneal Pharmaceuticals NYCarlsbad TechnologyPD-Rx PharmaceuticalsCouplerGolden State Medical SupplyHikma Pharmaceuticals14 labelers on the register
- Origin register
- US FDA, United States
- Storage
- Store at 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59° to 86°F).
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- J01MA02 Ciprofloxacin
- HS code (indicative)
- 3004.20Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 9 June 2004
- Identifiers
- RxCUI 197511, 197512, 309309DailyMed set ID 2b3b6a9f-259c-4736-b88f-f49d1eb64286, 37527eca-115e-4582-88cd-bba851ac6069, 5723eaf9-8659-4730-b792-4e4c33690ccb +15NDC 65862-078, 61442-224, 72789-125 +15Application ANDA077859, ANDA076126, ANDA076558 +4
Record updated 12 November 2026
Documents available
Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.
No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.
Packs
A sample of 40 packs from 14 labelers. The register lists 49 packs for this generic presentation, and we confirm the exact pack on the quote.
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 50 tablet, film coated in 1 bottle | 59651-873-50 | Aurobindo PharmaIndia | 9 February 2024 |
| 100 tablet, film coated in 1 bottle | 59651-978-01 | Aurobindo PharmaIndia | 27 March 2025 |
| 500 tablet, film coated in 1 bottle | 59651-978-05 | Aurobindo PharmaIndia | 27 March 2025 |
| 20 tablet, film coated in 1 bottle | 59651-978-20 | Aurobindo PharmaIndia | 27 March 2025 |
| 50 tablet, film coated in 1 bottle | 59651-978-50 | Aurobindo PharmaIndia | 27 March 2025 |
| 1000 tablet, film coated in 1 bottle | 59651-978-98 | Aurobindo PharmaIndia | 27 March 2025 |
| 50 tablet, film coated in 1 bottle | 65862-078-50 | Aurobindo PharmaIndia | 26 April 2007 |
| 100 tablet, film coated in 1 bottle | 69238-2434-1 | Amneal Pharmaceuticals NY | 29 February 2024 |
| 50 tablet, film coated in 1 bottle | 69238-2434-5 | Amneal Pharmaceuticals NY | 29 February 2024 |
| 400 tablet, film coated in 1 bottle | 61442-224-04 | Carlsbad Technology | 10 October 2009 |
| 50 tablet, film coated in 1 bottle | 61442-224-50 | Carlsbad Technology | 10 October 2009 |
| 20 tablet, film coated in 1 bottle, plastic | 62135-310-20 | Chartwell RX | 13 April 2021 |
| 28 tablet, film coated in 1 bottle, plastic | 62135-310-28 | Chartwell RX | 13 April 2021 |
| 50 tablet, film coated in 1 bottle, plastic | 62135-310-50 | Chartwell RX | 13 April 2021 |
| 50 tablet, film coated in 1 bottle | 0143-9929-50 | Hikma Pharmaceuticals | 9 June 2004 |
| 50 tablet, film coated in 1 bottle | 16571-413-05 | Rising Pharma Holdings | 10 September 2004 |
| 100 tablet in 1 bottle | 85293-004-01 | Umasuto | 5 March 2025 |
| 20 tablet, film coated in 1 bottle | 63629-3868-1 | Bryant Ranch Prepack | 30 October 2008 |
| 28 tablet, film coated in 1 bottle | 63629-3868-2 | Bryant Ranch Prepack | 12 June 2009 |
| 14 tablet, film coated in 1 bottle | 63629-3868-3 | Bryant Ranch Prepack | 23 April 2013 |
| 30 tablet, film coated in 1 bottle | 63629-3868-4 | Bryant Ranch Prepack | 26 July 2011 |
| 60 tablet, film coated in 1 bottle | 63629-3868-5 | Bryant Ranch Prepack | 14 December 2010 |
| 10 tablet, film coated in 1 bottle | 63629-3868-6 | Bryant Ranch Prepack | 3 December 2013 |
| 90 tablet, film coated in 1 bottle | 63629-3868-7 | Bryant Ranch Prepack | 6 March 2023 |
| 20 tablet, film coated in 1 bottle | 71335-1024-1 | Bryant Ranch Prepack | 28 December 2018 |
| 28 tablet, film coated in 1 bottle | 71335-1024-2 | Bryant Ranch Prepack | 28 December 2021 |
| 14 tablet, film coated in 1 bottle | 71335-1024-3 | Bryant Ranch Prepack | 10 December 2018 |
| 30 tablet, film coated in 1 bottle | 71335-1024-4 | Bryant Ranch Prepack | 28 December 2021 |
| 60 tablet, film coated in 1 bottle | 71335-1024-5 | Bryant Ranch Prepack | 28 December 2021 |
| 10 tablet, film coated in 1 bottle | 71335-1024-6 | Bryant Ranch Prepack | 11 December 2018 |
| 90 tablet, film coated in 1 bottle | 71335-1024-7 | Bryant Ranch Prepack | 28 December 2021 |
| 28 tablet in 1 bottle, plastic | 43063-767-28 | PD-Rx Pharmaceuticals | 19 May 2017 |
| 50 tablet, film coated in 1 bottle, plastic | 72789-125-50 | PD-Rx Pharmaceuticals | 7 October 2020 |
| 30 tablet in 1 blister pack | 67046-1528-3 | Coupler | 10 March 2025 |
| 50 tablet, film coated in 1 bottle | 51407-776-50 | Golden State Medical Supply | 7 May 2024 |
| 6 tablet, film coated in 1 bottle | 85534-0081-0 | Hawaii Repack | 26 April 2007 |
| 10 tablet, film coated in 1 bottle | 85534-0081-1 | Hawaii Repack | 26 April 2007 |
| 14 tablet, film coated in 1 bottle | 85534-0081-2 | Hawaii Repack | 26 April 2007 |
| 20 tablet, film coated in 1 bottle | 85534-0081-3 | Hawaii Repack | 26 April 2007 |
| 21 tablet, film coated in 1 bottle | 85534-0081-4 | Hawaii Repack | 26 April 2007 |
Status by register
Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 22 October 1987 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Import route
Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.
Import guides are available for 25 countries. Pick one to see its route summary.
BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides
Other strengths and forms of Ciprofloxacin
Clinical summary
Ciprofloxacin is a fluoroquinolone antibacterial indicated in adults (18 years of age and older) with infections caused by designated, susceptible bacteria and in pediatric patients where indicated, among other approved uses. MedsAcross supplies Ciprofloxacin for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
Read about CiprofloxacinFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Cipro prescribing information (Bayer HealthCare Pharmaceuticals) · U.S. National Library of Medicine, DailyMed
Need Ciprofloxacin 750 mg tablet for your hospital or patient?
Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.