testosterone cypionate
- Product NDC
- 50090-7584
- 11-digit product format
- 500907584
- Labeler code
- 50090
- Product ID
- 50090-7584_ef98b549-e131-4b8f-9490-5149774e4ba1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- testosterone cypionate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- A-S Medication Solutions
- Application
- ANDA215351
- Marketing category
- ANDA
- Marketing start
- 2024-11-01
- 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 |
|---|
| 50090-7584-0 | 50090758400 | 1 VIAL, SINGLE-DOSE in 1 CARTON (50090-7584-0) / 1 mL in 1 VIAL, SINGLE-DOSE | 2025-06-25 | No | No | Historical |