Propranolol Hydrochloride
- Product NDC
- 49999-286
- 11-digit product format
- 499990286
- Labeler code
- 49999
- Product ID
- 49999-286_e9f55f9b-4598-4456-bc54-8ed4dde8f1dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2012-03-23
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 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