testosterone cypionate
- Product NDC
- 72603-286
- 11-digit product format
- 726030286
- Labeler code
- 72603
- Product ID
- 72603-286_3ba42272-97f6-0e87-e063-6394a90a2d9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- testosterone cypionate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- NorthStar Rx LLC
- 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 |
|---|
| 72603-286-01 | 72603028601 | 1 VIAL, SINGLE-DOSE in 1 CARTON (72603-286-01) / 1 mL in 1 VIAL, SINGLE-DOSE | 2024-11-01 | No | No | Historical |