testosterone
- Product NDC
- 72162-1421
- 11-digit product format
- 721621421
- Labeler code
- 72162
- Product ID
- 72162-1421_78ca5df2-0a66-41fe-9f28-4ba270cfce81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- testosterone
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204255
- Marketing category
- ANDA
- Marketing start
- 2017-06-28
- Substance
- TESTOSTERONE
- Active strength
- 30 mg/1.5mL
- 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 |
|---|
| 3XMK78S47O | TESTOSTERONE | 58-22-0 | TESTOSTERONE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1421-2 | 72162142102 | 1 BOTTLE, PUMP in 1 CARTON (72162-1421-2) / 110 mL in 1 BOTTLE, PUMP | 2024-01-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| testosterone | Bryant Ranch Prepack | 2024-10-22 | HUMAN PRESCRIPTION DRUG LABEL | 105 |