Epinephrine
- Product NDC
- 50090-4544
- 11-digit product format
- 500904544
- Labeler code
- 50090
- Product ID
- 50090-4544_d3eafb4a-44b3-4e43-a53c-f9918e654846
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Epinephrine
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; SUBCUTANEOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA090589
- Marketing category
- ANDA
- Marketing start
- 2018-11-27
- Marketing end
- 0000-00-00
- Substance
- EPINEPHRINE
- Active strength
- 0 mg/.3mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4544-0 | 50090454400 | 2 CONTAINER in 1 CARTON (50090-4544-0) > 1 mL in 1 CONTAINER | 2 container | 2019-09-20 | 0000-00-00 | No | No | Current |