Epinephrine
- Product NDC
- 0517-3030
- 11-digit product format
- 005173030
- Labeler code
- 0517
- Product ID
- 0517-3030_495f1aad-cf64-41ab-9f9e-59f6ebeb44aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- epinephrine
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- American Regent, Inc.
- Application
- ANDA217192
- Marketing category
- ANDA
- Marketing start
- 2024-10-09
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Epinephrine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EPINEPHRINE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YKH834O4BH |
| Rxcui | 310132 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0517-3030-01 | Epinephrine | 1 mL in 1 VIAL | INJECTION | 1 | | 3 |
| 0517-3030-01 | Epinephrine | 01 in 1 CARTON | INJECTION | 01 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0517-3030 | EPINEPHRINE INJECTION [AMERICAN REGENT, INC.] | 3 | Current NDC, 2 package rows | 20241010_61cacda5-64ee-45ca-b94c-e8640c43e581.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0517-3030-01 | 00517303001 | 1 VIAL in 1 CARTON (0517-3030-01) / 1 mL in 1 VIAL | 1 vial | 2024-10-09 | No | No | Historical |