Pilocarpine hydrochloride
- Product NDC
- 68151-3015
- 11-digit product format
- 681513015
- Labeler code
- 68151
- Product ID
- 68151-3015_51e83b06-4fcc-4b9b-ba25-b0844015acff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pilocarpine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- NDA020237
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2011-09-13
- 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
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-3015-0 | Pilocarpine hydrochloride | 1 in 1 PACKAGE | TABLET, FILM COATED | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-3015 | PILOCARPINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160311_75fb8a60-bdba-4805-9c32-94377d1eb67f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-3015-0 | 68151301500 | 1 in 1 PACKAGE | Historical |