Propranolol Hydrochloride
- Product NDC
- 68788-7791
- 11-digit product format
- 687887791
- Labeler code
- 68788
- Product ID
- 68788-7791_8d251c03-02c2-4dff-942c-8133bcb99925
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA070322
- Marketing category
- ANDA
- Marketing start
- 2020-10-21
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F8A3652H1V |
| Rxcui | 856457 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-7791-3 | Propranolol Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7791 | PROPRANOLOL HYDROCHLORIDE TABLET [PREFERRED PHARMACEUTICALS INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240805_582fe781-0759-4622-8fa6-b7d90e94e696.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 |
|---|
| 68788-7791-3 | 68788779103 | 30 TABLET in 1 BOTTLE (68788-7791-3) | 30 tablet | 2020-10-21 | 0000-00-00 | No | No | Current |