Testosterone Cypionate
- Product NDC
- 76420-746
- 11-digit product format
- 764200746
- Labeler code
- 76420
- Product ID
- 76420-746_1a9699dd-3fd3-2a4e-e063-6294a90aa662
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Testosterone Cypionate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA091244
- Marketing category
- ANDA
- Marketing start
- 2019-03-26
- 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 |
|---|
| 76420-746-01 | 76420074601 | 1 VIAL, GLASS in 1 CARTON (76420-746-01) / 1 mL in 1 VIAL, GLASS | 2024-06-11 | No | No | Historical |
| 76420-746-10 | 76420074610 | 1 VIAL, GLASS in 1 CARTON (76420-746-10) / 10 mL in 1 VIAL, GLASS | 2024-06-11 | No | No | Historical |