Propranolol Hydrochloride
- Product NDC
- 43478-903
- 11-digit product format
- 434780903
- Labeler code
- 43478
- Product ID
- 43478-903_54753570-5982-418f-acea-aabf39c8a50b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Rouses Point Pharm
- Application
- NDA018553
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2009-02-25
- Marketing end
- 2019-09-30
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record