Proparacaine Hydrochloride
- Product NDC
- 68071-4701
- 11-digit product format
- 680714701
- Labeler code
- 68071
- Product ID
- 68071-4701_bb8bf375-9d5c-d538-e053-2995a90a65f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Proparacaine Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA080027
- Marketing category
- ANDA
- Marketing start
- 2000-06-05
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4701-5 | 68071470105 | 15 mL in 1 BOTTLE (68071-4701-5) | 15 ml | 2019-01-08 | 0000-00-00 | No | No | Current |