EPINEPHRINE
- Product NDC
- 72572-235
- 11-digit product format
- 725720235
- Labeler code
- 72572
- Product ID
- 72572-235_2099a4b3-66ca-4e01-a9e6-4790b538ec22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- EPINEPHRINE
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAMUSCULAR; INTRAOCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- CIVICA, INC.
- Application
- ANDA213708
- Marketing category
- ANDA
- Marketing start
- 2024-11-21
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- EPINEPHRINE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EPINEPHRINE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YKH834O4BH |
| Rxcui | 1660014 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72572-235-01 | EPINEPHRINE | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION, CONCENTRATE | 1 | | 1 |
| 72572-235-25 | EPINEPHRINE | 25 in 1 TRAY | INJECTION, SOLUTION, CONCENTRATE | 25 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72572-235-01 | 72572023501 | 1 mL in 1 VIAL, SINGLE-DOSE | 1 ml | | | | Historical |
| 72572-235-25 | 72572023525 | 25 VIAL, SINGLE-DOSE in 1 TRAY (72572-235-25) / 1 mL in 1 VIAL, SINGLE-DOSE (72572-235-01) | | 2024-11-21 | No | No | Current |