SYMJEPI
- Product NDC
- 0781-3442
- 11-digit product format
- 007813442
- Labeler code
- 0781
- Product ID
- 0781-3442_683751b5-3deb-4292-b7e8-96f68bd09f0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Epinephrine
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; SUBCUTANEOUS
- Labeler
- Sandoz Inc.
- Application
- NDA207534
- Marketing category
- NDA
- Marketing start
- 2018-12-07
- Marketing end
- 0000-00-00
- Substance
- EPINEPHRINE
- Active strength
- 0 mg/.3mL
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-3442-20 | 00781344220 | 2 SYRINGE in 1 CARTON (0781-3442-20) > .3 mL in 1 SYRINGE | 2 syringe | 2018-12-07 | 2021-07-31 | No | No | Current |