Propranolol Hydrochloride
- Product NDC
- 50090-7618
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078955
- Marketing category
- ANDA
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-7618-1 | 60 TABLET in 1 BOTTLE (50090-7618-1) | 2025-08-01 | No | Historical | |
| 50090-7618-6 | 90 TABLET in 1 BOTTLE (50090-7618-6) | 2025-08-01 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Propranolol Hydrochloride Tablets, USP | A-S Medication Solutions | 2025-08-08 | HUMAN PRESCRIPTION DRUG LABEL | 2 |