Depo-Testosterone
- Product NDC
- 0009-0520
- 11-digit product format
- 000090520
- Labeler code
- 0009
- Product ID
- 0009-0520_1c676fa2-222b-4723-aedf-0cbb5c7da935
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- testosterone cypionate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Pharmacia and Upjohn Company LLC
- Application
- ANDA085635
- Marketing category
- ANDA
- Marketing start
- 2014-03-31
- Marketing end
- 0000-00-00
- Substance
- TESTOSTERONE CYPIONATE
- Active strength
- 200 mg/mL
- Pharmacologic classes
- Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record