Testosterone Cypionate
- Product NDC
- 50090-0330
- 11-digit product format
- 500900330
- Labeler code
- 50090
- Product ID
- 50090-0330_939a3a4a-c758-4cd0-b147-68592caa7f70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Testosterone Cypionate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- A-S Medication Solutions
- Application
- ANDA091244
- Marketing category
- ANDA
- Marketing start
- 2012-05-01
- Marketing end
- 0000-00-00
- Substance
- TESTOSTERONE CYPIONATE
- Active strength
- 200 mg/mL
- Pharmacologic classes
- Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0330-0 | 50090033000 | 10 mL in 1 VIAL (50090-0330-0) | 10 ml | 2014-11-28 | 0000-00-00 | No | No | Current |