Medicine
Polocaine 51 mg/1.7 mL injection
Polocaine 51 mg/1.7 mL injection is a prescription medicine containing Mepivacaine for submucosal use, marketed by Dentsply Pharmaceutical, 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
Do not permit to freeze. Both solutions should be stored at controlled room…
Key facts
- Active ingredient (INN)
- Mepivacaine
- Brand
- Polocaine
- Strength
- 51 mg/1.7 mL
- Dosage form
- Injection
- Route
- Submucosal
- Packs
- 50 cartridges of 1.7 mL
- Marketing authorisation holder
- Dentsply Pharmaceutical
- Manufacturers
- Dentsply PharmaceuticalNovocol Pharmaceutical of Canada
- Origin register
- US FDA, United States
- Storage
- Do not permit to freeze. Both solutions should be stored at controlled room temperature, below 25° C (77° F). Protect from light.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- N01BB03 Mepivacaine
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 10 October 1984
- Identifiers
- RxCUI 1012756, 1305263DailyMed set ID 25074a6a-7f67-4ad8-86e0-2afe23ec5d04, eb7e2284-fe8d-46ad-b1d3-92ee2c6222bfNDC 66312-441, 51004-4411Application ANDA088387
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
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 50 cartridge in 1 carton / 1.7 mL in 1 cartridge | 66312-441-16 | Dentsply Pharmaceutical | 10 October 1984 |
| 50 cartridge in 1 carton / 1.7 mL in 1 cartridge | 51004-4411-6 | Novocol Pharmaceutical of Canada | 10 October 1984 |
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 6 January 1960 | 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
Alternatives
Other makers and brands of Mepivacaine 51 mg/1.7 mL injection.
Other strengths and forms of Mepivacaine
Clinical summary
Mepivacaine is an amide local anesthetic indicated for production of local anesthesia for dental procedures by infiltration or nerve block in adults and pediatric patients. It is available as injection for submucosal, infiltration and epidural use. MedsAcross supplies Mepivacaine 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 MepivacaineFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Scandonest 3% Plain prescribing information (Septodont) · U.S. National Library of Medicine, DailyMed
Need Polocaine 51 mg/1.7 mL injection 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.