Proparacaine Hydrochloride
- Product NDC
- 70518-2056
- 11-digit product format
- 705182056
- Labeler code
- 70518
- Product ID
- 70518-2056_87db898e-f1ce-90a1-e053-2a95a90a0a37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Proparacaine Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040277
- Marketing category
- ANDA
- Marketing start
- 2019-05-01
- Marketing end
- 0000-00-00
- Substance
- PROPARACAINE HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Local Anesthesia [PE],Local Anesthetic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record