Propranolol Hydrochloride
- Product NDC
- 50090-7101
- 11-digit product format
- 500907101
- Labeler code
- 50090
- Product ID
- 50090-7101_e066fdd7-a8bc-4cc5-88e6-1c6556bac6dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071972
- Marketing category
- ANDA
- Marketing start
- 2021-06-03
- 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 |
|---|
| 50090-7101-1 | 50090710101 | 100 TABLET in 1 BOTTLE (50090-7101-1) | 100 tablet | 2024-02-29 | No | No | Historical |
| 50090-7101-6 | 50090710106 | 90 TABLET in 1 BOTTLE (50090-7101-6) | 90 tablet | 2024-02-29 | No | No | Historical |