Pilocarpine Hydrochloride
- Product NDC
- 21695-601
- 11-digit product format
- 216950601
- Labeler code
- 21695
- Product ID
- 21695-601_f168b0a9-4e9a-47f7-b391-edcea871956e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pilocarpine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA077248
- Marketing category
- ANDA
- Marketing start
- 2006-03-31
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-601-90 | Pilocarpine Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-601 | PILOCARPINE HYDROCHLORIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20101119_f168b0a9-4e9a-47f7-b391-edcea871956e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-601-90 | 21695060190 | 90 in 1 BOTTLE | Historical |