Epinephrine
- Product NDC
- 70518-1215
- 11-digit product format
- 705181215
- Labeler code
- 70518
- Product ID
- 70518-1215_d9171343-f5a0-1663-e053-2995a90a4b3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Epinephrine
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- NDA205029
- Marketing category
- NDA
- Marketing start
- 2018-05-17
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1215 | EPINEPHRINE INJECTION, SOLUTION, CONCENTRATE [REMEDYREPACK INC.] | 12 | Legacy NDC | 20250508_a9597463-896e-4fd4-bfd5-902f6736a54d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1215-0 | 70518121500 | 10 AMPULE in 1 BOX (70518-1215-0) > 1 mL in 1 AMPULE | 10 ampule | 2018-05-17 | 0000-00-00 | No | No | Current |