Propranolol Hydrochloride
- Product NDC
- 68071-2710
- 11-digit product format
- 680712710
- Labeler code
- 68071
- Product ID
- 68071-2710_127807d8-587c-49c7-e063-6294a90a0e43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA070322
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- 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 |
|---|
| 68071-2710-3 | 68071271003 | 30 TABLET in 1 BOTTLE (68071-2710-3) | 30 tablet | 2022-05-19 | No | No | Historical |
| 68071-2710-9 | 68071271009 | 90 TABLET in 1 BOTTLE (68071-2710-9) | 90 tablet | 2022-05-19 | No | No | Historical |