Propranolol Hydrochloride
- Product NDC
- 68788-8595
- 11-digit product format
- 687888595
- Labeler code
- 68788
- Product ID
- 68788-8595_fc5cc977-a36b-4324-a4a6-7cfbd1fb0363
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA071972
- Marketing category
- ANDA
- Marketing start
- 2024-03-01
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 20 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 |
|---|
| 68788-8595-3 | 68788859503 | 30 TABLET in 1 BOTTLE (68788-8595-3) | 30 tablet | 2024-03-01 | No | No | Historical |
| 68788-8595-9 | 68788859509 | 90 TABLET in 1 BOTTLE (68788-8595-9) | 90 tablet | 2024-03-01 | No | No | Historical |