Anadrol-50
- Product NDC
- 68220-055
- 11-digit product format
- 682200055
- Labeler code
- 68220
- Product ID
- 68220-055_87e8308b-0b5c-4572-b373-9e8e607f1f1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxymetholone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Alaven Pharmaceutical LLC
- Application
- NDA016848
- Marketing category
- NDA
- Marketing start
- 1972-06-01
- Marketing end
- 0000-00-00
- Substance
- OXYMETHOLONE
- Active strength
- 50 mg/1
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68220-055-10 | 68220005510 | 1 BOTTLE in 1 CARTON (68220-055-10) > 100 TABLET in 1 BOTTLE | 1 bottle | 1972-06-01 | 0000-00-00 | No | No | Current |