Adenosine
- Product NDC
- 0703-8777
- 11-digit product format
- 007038777
- Labeler code
- 0703
- Product ID
- 0703-8777_6e64c28a-1348-431d-a547-1d4d016eb4d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Adenosine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA077425
- Marketing category
- ANDA
- Marketing start
- 2013-09-23
- Marketing end
- 0000-00-00
- Substance
- ADENOSINE
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Adenosine Receptor Agonist [EPC],Adenosine Receptor Agonists [MoA]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0703-8777-01 | 00703877701 | 1 VIAL, SINGLE-USE in 1 CARTON (0703-8777-01) > 30 mL in 1 VIAL, SINGLE-USE | 2013-09-23 | 0000-00-00 | No | No | Current |