Propranolol Hydrochloride
- Product NDC
- 72162-1175
- 11-digit product format
- 721621175
- Labeler code
- 72162
- Product ID
- 72162-1175_088d7e29-6c0b-4377-9c45-f2fa8b58c27d
- 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
- 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
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 |
|---|
| 72162-1175-0 | 72162117500 | 1000 TABLET in 1 BOTTLE (72162-1175-0) | 1000 tablet | 2024-10-04 | No | No | Historical |
| 72162-1175-1 | 72162117501 | 60 TABLET in 1 BOTTLE (72162-1175-1) | 60 tablet | 2023-06-26 | No | No | Historical |