EPINEPHRINE
- Product NDC
- 52584-103
- 11-digit product format
- 525840103
- Labeler code
- 52584
- Product ID
- 52584-103_0ed5aad6-c31b-42f8-8130-318e308d3e60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- EPINEPHRINE
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- NDA205029
- Marketing category
- NDA
- Marketing start
- 2018-07-02
- Marketing end
- 2023-07-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-103-01 | 52584010301 | 1 AMPULE in 1 BAG (52584-103-01) > 1 mL in 1 AMPULE | 1 ampule | 2018-07-02 | 2023-07-31 | No | No | Current |