Propranolol Hydrochloride
- Product NDC
- 70518-4471
- 11-digit product format
- 705184471
- Labeler code
- 70518
- Product ID
- 70518-4471_3e5df9b1-1506-1ebd-e063-6294a90a12ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2025-09-09
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 70518-4471-0 | 70518447100 | 30 TABLET in 1 BLISTER PACK (70518-4471-0) | 30 tablet | 2025-09-09 | No | No | Historical |