Propranolol Hydrochloride
- Product NDC
- 50090-7620
- 11-digit product format
- 500907620
- Labeler code
- 50090
- Product ID
- 50090-7620_02d755ba-6993-4d01-aabe-33b06d56d4c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2024-09-19
- 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 |
|---|
| 50090-7620-0 | 50090762000 | 30 TABLET in 1 BOTTLE (50090-7620-0) | 30 tablet | 2025-08-01 | No | No | Historical |
| 50090-7620-1 | 50090762001 | 100 TABLET in 1 BOTTLE (50090-7620-1) | 100 tablet | 2025-08-01 | No | No | Historical |
| 50090-7620-6 | 50090762006 | 90 TABLET in 1 BOTTLE (50090-7620-6) | 90 tablet | 2025-08-01 | No | No | Historical |