Pindolol
- Product NDC
- 76385-132
- 11-digit product format
- 763850132
- Labeler code
- 76385
- Product ID
- 76385-132_9b26764d-3ed0-4cb8-8740-355800dc62e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pindolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Application
- ANDA211712
- Marketing category
- ANDA
- Marketing start
- 2020-02-01
- Substance
- PINDOLOL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pindolol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PINDOLOL | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | BJ4HF6IU1D |
| Rxcui | 198104, 198105 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76385-132-01 | Pindolol | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76385-132 | PINDOLOL TABLET [BAYSHORE PHARMACEUTICALS LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20200205_f529ff35-f82b-4a3a-96b4-096bfc8e81b5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76385-132-01 | 76385013201 | 100 TABLET in 1 BOTTLE, PLASTIC (76385-132-01) | 100 tablet | 2020-02-01 | 0000-00-00 | No | No | Current |