Propranolol Hydrochloride
- Product NDC
- 72162-1178
- 11-digit product format
- 721621178
- Labeler code
- 72162
- Product ID
- 72162-1178_215b3a31-7efd-4b68-82ca-a6b8f3e8b1fb
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F8A3652H1V | PROPRANOLOL HYDROCHLORIDE | 318-98-9 | PROPRANOLOL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1178-1 | 72162117801 | 100 TABLET in 1 BOTTLE (72162-1178-1) | 100 tablet | 2024-10-04 | No | No | Historical |