pilocarpine Hydrochloride
- Product NDC
- 69292-275
- 11-digit product format
- 692920275
- Labeler code
- 69292
- Product ID
- 69292-275_731fb0fb-3a68-40bc-ae79-3c4b0ac81cfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PILOCARPINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AMICI PHARMACEUTICALS LLC
- Application
- ANDA076963
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- Marketing end
- 0000-00-00
- Substance
- PILOCARPINE HYDROCHLORIDE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Cholinergic Agonists [MoA],Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69292-275-10 | 69292027510 | 100 TABLET, FILM COATED in 1 BOTTLE (69292-275-10) | 2018-10-01 | 0000-00-00 | No | No | Current |
| 69292-275-50 | 69292027550 | 500 TABLET, FILM COATED in 1 BOTTLE (69292-275-50) | 2018-10-01 | 0000-00-00 | No | No | Current |