Pilocarpine Hydrochloride
- Product NDC
- 60219-5922
- 11-digit product format
- 602195922
- Labeler code
- 60219
- Product ID
- 60219-5922_83bbaf17-9d8e-494a-8e76-361550296b5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PILOCARPINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA077248
- Marketing category
- ANDA
- Marketing start
- 2007-05-01
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pilocarpine Hydrochloride
- Listing expiration
- 2027-12-31
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 |
|---|
| 60219-5922-1 | Pilocarpine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60219-5922 | PILOCARPINE HYDROCHLORIDE TABLET, FILM COATED [AMNEAL PHARMACEUTICALS NY LLC] | 16 | Current NDC, Legacy NDC, 1 package rows | 20231229_6272ccac-b543-404d-9938-8583bb59ed2c.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 |
|---|
| 60219-5922-1 | 60219592201 | 100 TABLET, FILM COATED in 1 BOTTLE (60219-5922-1) | 2007-05-01 | 0000-00-00 | No | No | Current |