Propranolol Hydrochloride
- Product NDC
- 50090-7263
- 11-digit product format
- 500907263
- Labeler code
- 50090
- Product ID
- 50090-7263_152ccf8d-9d06-4ba2-bc76-ae5b11579d47
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA212026
- Marketing category
- ANDA
- Marketing start
- 2020-01-06
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 80 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7263-0 | 50090726300 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7263-0) | 2024-10-03 | No | No | Historical |