Testosterone Cypionate
- Product NDC
- 69761-312
- 11-digit product format
- 697610312
- Labeler code
- 69761
- Product ID
- 69761-312_7378dc78-63df-48d4-88e7-ab0043753377
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Testosterone Cypionate
- Dosage form
- SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Qualgen LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-01-02
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69761-312-11 | 69761031211 | 1 VIAL, GLASS in 1 BOX (69761-312-11) > 10 mL in 1 VIAL, GLASS | 2021-01-02 | 0000-00-00 | No | No | Current |