epinephrine
- Product NDC
- 50090-1360
- 11-digit product format
- 500901360
- Labeler code
- 50090
- Product ID
- 50090-1360_8762adbc-29bb-47d0-b094-8dd0e4aa2a5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- epinephrine
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- A-S Medication Solutions
- Application
- NDA020800
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2010-04-01
- Marketing end
- 0000-00-00
- Substance
- EPINEPHRINE
- Active strength
- 0 mg/.3mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record