Adrenalin
- Product NDC
- 52584-159
- 11-digit product format
- 525840159
- Labeler code
- 52584
- Product ID
- 52584-159_41c6894d-f8e8-4242-96a5-819d4f322155
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- epineprine
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- NDA204200
- Marketing category
- NDA
- Marketing start
- 2019-08-13
- Marketing end
- 2024-01-31
- Substance
- EPINEPHRINE
- Active strength
- 1 mg/mL
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-159-25 | 52584015925 | 1 VIAL, SINGLE-USE in 1 BAG (52584-159-25) > 1 mL in 1 VIAL, SINGLE-USE | 2019-08-13 | 2024-01-31 | No | No | Current |