pilocarpine hydrchloride
- Product NDC
- 71335-2120
- 11-digit product format
- 713352120
- Labeler code
- 71335
- Product ID
- 71335-2120_fda30c73-7230-bbca-e053-6294a90ae203
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pilocarpine hydrchloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076746
- Marketing category
- ANDA
- Marketing start
- 2020-08-24
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- pilocarpine hydrchloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PILOCARPINE HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0WW6D218XJ |
| Rxcui | 1000913 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2120-1 | pilocarpine hydrchloride | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2120 | PILOCARPINE HYDRCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 101 | Current NDC, Legacy NDC, 1 package rows | 20230609_2a646f09-72e3-4795-8e69-40fb84d04a4f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2120-1 | 71335212001 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2120-1) | 2022-06-20 | 0000-00-00 | No | No | Current |