Propranolol Hydrochloride
- Product NDC
- 72789-423
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA071972
- Marketing category
- ANDA
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72789-423-30 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-423-30) | 2024-07-12 | | No | Historical |
| 72789-423-60 | 60 TABLET in 1 BOTTLE, PLASTIC (72789-423-60) | 2024-12-23 | | No | Historical |
| 72789-423-90 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-423-90) | 2025-06-03 | | No | Historical |