Minoxidil
- Product NDC
- 72882-094
- 11-digit product format
- 728820094
- Labeler code
- 72882
- Product ID
- 72882-094_bdba5fcf-cb9d-4904-b234-d42d7c7af606
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Mens LLC
- Application
- ANDA075518
- Marketing category
- ANDA
- Marketing start
- 2020-05-21
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72882-094-73 | 72882009473 | 1 BOTTLE, DROPPER in 1 CARTON (72882-094-73) > 60 mL in 1 BOTTLE, DROPPER | 2020-05-21 | 0000-00-00 | No | No | Current |