EPINEPHRINE
- Product NDC
- 51662-1629
- 11-digit product format
- 516621629
- Labeler code
- 51662
- Product ID
- 51662-1629_0f92ce97-4440-685c-e063-6394a90a637e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- EPINEPHRINE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA211363
- Marketing category
- NDA
- Marketing start
- 2023-04-20
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YKH834O4BH | EPINEPHRINE | 51-43-4 | EPINEPHRINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51662-1629-1 | 51662162901 | 1 SYRINGE in 1 BOX (51662-1629-1) / 10 mL in 1 SYRINGE | 1 syringe | 2023-04-20 | No | No | Historical |
| 51662-1629-3 | 51662162903 | 10 POUCH in 1 CASE (51662-1629-3) / 1 BOX in 1 POUCH (51662-1629-2) / 1 SYRINGE in 1 BOX / 10 mL in 1 SYRINGE | 10 pouch | 2023-04-20 | No | No | Historical |