adenosine
- Product NDC
- 70518-2778
- 11-digit product format
- 705182778
- Labeler code
- 70518
- Product ID
- 70518-2778_baea0383-2f72-617c-e053-2995a90ab25c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- adenosine
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078686
- Marketing category
- ANDA
- Marketing start
- 2020-06-11
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| K72T3FS567 | ADENOSINE | 58-61-7 | ADENOSINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2778-1 | 70518277801 | 10 VIAL, SINGLE-DOSE in 1 CARTON (70518-2778-1) > 2 mL in 1 VIAL, SINGLE-DOSE (70518-2778-0) | 2020-06-11 | 0000-00-00 | No | No | Current |