Medicine
Minocycline 75 mg tablet
Minocycline 75 mg tablet is a generic prescription medicine for oral use, made by 4 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). Protect from light, moisture and excessive…
Key facts
- Active ingredient (INN)
- Minocycline
- Brand
- Sold under the generic name
- Strength
- 75 mg
- Dosage form
- Tablet
- Route
- Oral
- Packs
- 100 tablets, 60 tablets and 1 more
- Manufacturers
- Aurobindo PharmaIndiaStrides PharmaIndiaTorrent PharmaceuticalsIndiaChartwell RX
- Origin register
- US FDA, United States
- Storage
- Store at 20° to 25°C (68° to 77°F). Protect from light, moisture and excessive heat.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- A01AB23 Minocycline
- HS code (indicative)
- 3004.20Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 26 December 2007
- Identifiers
- RxCUI 207362, 207364, 403840DailyMed set ID d6e136ba-c9b1-4846-ae2a-98a29cb4504d, 3539f84e-b489-4914-96c1-ac3731032971, 799a9871-3249-471e-b88d-5d8f7d4b96ad +1NDC 64380-155, 13668-486, 59651-338 +1Application ANDA065131, ANDA065156, ANDA213662 +1
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
Packs from every labeler of this generic presentation.
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 100 tablet, film coated in 1 container | 59651-338-01 | Aurobindo PharmaIndia | 1 May 2020 |
| 100 tablet in 1 bottle | 64380-155-01 | Strides PharmaIndia | 11 April 2022 |
| 100 tablet in 1 bottle | 13668-486-01 | Torrent PharmaceuticalsIndia | 2 April 2015 |
| 60 tablet in 1 bottle | 62135-888-60 | Chartwell RX | 13 June 2025 |
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 30 June 1971 | 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 Minocycline
Clinical summary
Minocycline is a tetracycline-class drug indicated in the treatment of infections due to susceptible isolates of the designated bacteria, among other approved uses. MedsAcross supplies Minocycline 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 MinocyclineFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Minocin prescribing information (Melinta Therapeutics) · U.S. National Library of Medicine, DailyMed
Need Minocycline 75 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.