Propranolol Hydrochloride
- Product NDC
- 50090-0147
- 11-digit product format
- 500900147
- Labeler code
- 50090
- Product ID
- 50090-0147_482b54d9-3d6c-4367-8329-f45ed44151ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2008-10-13
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record