Minoxidil
- Product NDC
- 11822-0129
- 11-digit product format
- 118220129
- Labeler code
- 11822
- Product ID
- 11822-0129_30d7818b-1d83-44e4-bfb9-a33067a30dd8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA091344
- Marketing category
- ANDA
- Marketing start
- 2017-03-09
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 11822-0129-1 | 11822012901 | 1 CAN in 1 CARTON (11822-0129-1) > 60 g in 1 CAN | 1 can | 2020-09-25 | 0000-00-00 | No | No | Current |
| 11822-0129-2 | 11822012902 | 2 CAN in 1 CARTON (11822-0129-2) > 60 g in 1 CAN | 2 can | 2017-03-09 | 0000-00-00 | No | No | Current |