Propranolol Hydrochloride
- Product NDC
- 71335-2299
- 11-digit product format
- 713352299
- Labeler code
- 71335
- Product ID
- 71335-2299_0973b288-7f06-4c22-ae38-9fc16865d18f
- 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
- 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
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 |
|---|
| 71335-2299-1 | 71335229901 | 1000 TABLET in 1 BOTTLE (71335-2299-1) | 1000 tablet | 2024-10-04 | No | No | Historical |