Pilocarpine Hydrochloride
- Product NDC
- 71335-2094
- 11-digit product format
- 713352094
- Labeler code
- 71335
- Product ID
- 71335-2094_e08f99ec-9d2a-4af2-8554-2a8da6b1916a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pilocarpine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212377
- Marketing category
- ANDA
- Marketing start
- 2019-08-13
- Marketing end
- 0000-00-00
- Substance
- PILOCARPINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinergic Agonists [MoA], Cholinergic Muscarinic Agonists [MoA], Cholinergic Receptor Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2094-1 | 71335209401 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2094-1) | 2022-05-23 | 0000-00-00 | No | No | Current |