Propranolol Hydrochloride
- Product NDC
- 60760-731
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA071972
- Marketing category
- ANDA
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 60760-731-60 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-731-60) | 2025-11-05 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Propranolol Hydrochloride Tablets, USP (10 mg, 20 mg, 40 mg, 60 mg and 80 mg) Rx Only | ST. MARY'S MEDICAL PARK PHARMACY | 2025-11-05 | HUMAN PRESCRIPTION DRUG LABEL | 1 |