Epinephrine
- Product NDC
- 50090-2733
- 11-digit product format
- 500902733
- Labeler code
- 50090
- Product ID
- 50090-2733_aaeb2e08-e729-48ef-a6a4-8d4a66cf2e6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Epinephrine
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- A-S Medication Solutions
- Application
- NDA019430
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-12-15
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#