Testosterone Cypionate
- Product NDC
- 71335-2473
- 11-digit product format
- 713352473
- Labeler code
- 71335
- Product ID
- 71335-2473_875e1ce9-4be2-442c-a869-db81a43d2a43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Testosterone Cypionate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040530
- Marketing category
- ANDA
- Marketing start
- 2007-12-21
- Substance
- TESTOSTERONE CYPIONATE
- Active strength
- 200 mg/mL
- Pharmacologic classes
- Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| M0XW1UBI14 | TESTOSTERONE CYPIONATE | 58-20-8 | TESTOSTERONE CYPIONATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2473-1 | 71335247301 | 1 VIAL, GLASS in 1 CARTON (71335-2473-1) / 10 mL in 1 VIAL, GLASS | 2024-09-05 | No | No | Historical |