Pindolol
- Product NDC
- 63629-4828
- 11-digit product format
- 636294828
- Labeler code
- 63629
- Product ID
- 63629-4828_ddddec64-b3a3-4cf4-b9c6-b92d939f9df8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pindolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211712
- Marketing category
- ANDA
- Marketing start
- 2020-02-01
- Substance
- PINDOLOL
- Active strength
- 5 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 | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | BJ4HF6IU1D |
| Rxcui | 198105 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-4828-1 | Pindolol | 180 in 1 BOTTLE, PLASTIC | TABLET | 180 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-4828 | PINDOLOL TABLET [BRYANT RANCH PREPACK] | 1 | Current NDC, 1 package rows | 20241127_7fb36f8f-11fe-498e-8667-daeccf8b2273.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-4828-1 | 63629482801 | 180 TABLET in 1 BOTTLE, PLASTIC (63629-4828-1) | 180 tablet | 2024-11-25 | No | No | Historical |