Propranolol Hydrochloride
- Product NDC
- 50090-3302
- 11-digit product format
- 500903302
- Labeler code
- 50090
- Product ID
- 50090-3302_e929b165-b53c-40f5-bca1-a865b6cd4ae6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 2016-09-19
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record