Adenosine
- Product NDC
- 71288-207
- 11-digit product format
- 712880207
- Labeler code
- 71288
- Product ID
- 71288-207_0ad2efd3-3c6e-4cb8-8d82-3aa7ae84a81a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Adenosine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Meitheal Pharmaceuticals Inc.
- Application
- ANDA077425
- Marketing category
- ANDA
- Marketing start
- 2025-04-30
- Substance
- ADENOSINE
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Adenosine Receptor Agonist [EPC], Adenosine Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71288-207-21 | 71288020721 | 10 VIAL, SINGLE-USE in 1 CARTON (71288-207-21) / 20 mL in 1 VIAL, SINGLE-USE | 2025-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Adenosine | Meitheal Pharmaceuticals Inc. | 2025-04-14 | HUMAN PRESCRIPTION DRUG LABEL | 1 |