Minoxidil
- Product NDC
- 11822-0202
- 11-digit product format
- 118220202
- Labeler code
- 11822
- Product ID
- 11822-0202_4cadc133-acc0-483d-82d3-838707f3ef55
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2016-10-14
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0202 | MINOXIDIL SOLUTION [RITE AID CORPORATION] | 3 | Legacy NDC | 20210921_66189825-30a3-48b0-844f-645a0c16773a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0202-1 | 11822020201 | 3 BOTTLE in 1 CARTON (11822-0202-1) > 60 mL in 1 BOTTLE | 3 bottle | 2016-10-14 | 0000-00-00 | No | No | Current |