testosterone cypionate
- Product NDC
- 76420-747
- 11-digit product format
- 764200747
- Labeler code
- 76420
- Product ID
- 76420-747_1aaa41c9-f5ad-54c2-e063-6394a90a6cc5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- testosterone cypionate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA207742
- Marketing category
- ANDA
- Marketing start
- 2022-11-02
- 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 |
|---|
| 76420-747-01 | 76420074701 | 1 VIAL, SINGLE-DOSE in 1 CARTON (76420-747-01) / 1 mL in 1 VIAL, SINGLE-DOSE | 2024-06-12 | No | No | Historical |