Adenosine
- Product NDC
- 0409-1932
- 11-digit product format
- 004091932
- Labeler code
- 0409
- Product ID
- 0409-1932_af4ef593-85c4-472a-9d07-5cd821e25715
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ADENOSINE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA203883
- Marketing category
- ANDA
- Marketing start
- 2014-04-02
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-1932-01 | 00409193201 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1932-01) > 20 mL in 1 VIAL, SINGLE-DOSE | 2014-04-02 | 0000-00-00 | No | No | Current |
| 0409-1932-02 | 00409193202 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1932-02) > 30 mL in 1 VIAL, SINGLE-DOSE | 2014-04-02 | 0000-00-00 | No | No | Current |