minoxidil
- Product NDC
- 11822-1033
- 11-digit product format
- 118221033
- Labeler code
- 11822
- Product ID
- 11822-1033_695f63d4-820c-4b1b-bf8b-c7a2569d0fa3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2021-05-29
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 5 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5965120SH1 | MINOXIDIL | 38304-91-5 | MINOXIDIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-1033-0 | 11822103300 | 3 BOTTLE, DROPPER in 1 CARTON (11822-1033-0) > 60 mL in 1 BOTTLE, DROPPER | 2021-06-02 | 0000-00-00 | No | No | Current |
| 11822-1033-1 | 11822103301 | 1 BOTTLE, DROPPER in 1 CARTON (11822-1033-1) > 60 mL in 1 BOTTLE, DROPPER | 2021-05-29 | 0000-00-00 | No | No | Current |