Adenosine
- Product NDC
- 17478-542
- 11-digit product format
- 174780542
- Labeler code
- 17478
- Product ID
- 17478-542_8029cdd2-f38f-48da-af52-91064fc5fc26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Adenosine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA078076
- Marketing category
- ANDA
- Marketing start
- 2011-03-15
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-542-02 | 17478054202 | 10 VIAL in 1 CARTON (17478-542-02) > 2 mL in 1 VIAL | 10 vial | 2011-03-15 | 0000-00-00 | No | No | Current |
| 17478-542-25 | 17478054225 | 25 VIAL in 1 CARTON (17478-542-25) > 2 mL in 1 VIAL | 25 vial | 2011-03-15 | 0000-00-00 | No | No | Current |