epinephrine
- Product NDC
- 71872-7007
- 11-digit product format
- 718727007
- Labeler code
- 71872
- Product ID
- 71872-7007_9ce57b9f-9580-91b1-e053-2995a90a100c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- epinephrine
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- NDA020800
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2010-04-01
- Marketing end
- 0000-00-00
- Substance
- EPINEPHRINE
- Active strength
- 0 mg/.15mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7007-1 | 71872700701 | 1 CASE in 1 BAG (71872-7007-1) > 1 SYRINGE, GLASS in 1 CASE > .15 mL in 1 SYRINGE, GLASS | 1 case | 2018-02-28 | 0000-00-00 | No | No | Current |