Propranolol Hydrochloride
- Product NDC
- 63629-2280
- 11-digit product format
- 636292280
- Labeler code
- 63629
- Product ID
- 63629-2280_5db966fd-3f94-4fae-a3f1-301cd9865a87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070221
- Marketing category
- ANDA
- Marketing start
- 2010-06-21
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 60 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
- Propranolol Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROPRANOLOL HYDROCHLORIDE | 60 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F8A3652H1V |
| Rxcui | 856556 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-2280-1 | Propranolol Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 105 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2280 | PROPRANOLOL HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 105 | Current NDC, Legacy NDC, 1 package rows | 20241023_1c275a7b-2e85-4990-b3ad-6c675d6c2d7b.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 |
|---|
| 63629-2280-1 | 63629228001 | 100 TABLET in 1 BOTTLE (63629-2280-1) | 100 tablet | 2024-10-10 | 0000-00-00 | No | No | Current |