Testosterone Cypionate
- Product NDC
- 72162-2348
- 11-digit product format
- 721622348
- Labeler code
- 72162
- Product ID
- 72162-2348_06604c5c-8606-420a-a577-d8ad62a3012a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- testosterone cypionate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206368
- Marketing category
- ANDA
- Marketing start
- 2019-05-31
- 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 |
|---|
| 72162-2348-2 | 72162234802 | 1 VIAL, SINGLE-DOSE in 1 CARTON (72162-2348-2) / 1 mL in 1 VIAL, SINGLE-DOSE | 2019-05-31 | No | No | Historical |
| 72162-2348-4 | 72162234804 | 1 VIAL, MULTI-DOSE in 1 CARTON (72162-2348-4) / 10 mL in 1 VIAL, MULTI-DOSE | 2019-05-31 | No | No | Historical |