Minoxidil
- Product NDC
- 0472-0094
- 11-digit product format
- 004720094
- Labeler code
- 0472
- Product ID
- 0472-0094_f109d743-b84f-4da6-869a-826704419432
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA075518
- Marketing category
- ANDA
- Marketing start
- 2000-11-20
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0472-0094-73 | 00472009473 | 1 BOTTLE, DROPPER in 1 CARTON (0472-0094-73) > 60 mL in 1 BOTTLE, DROPPER | 2000-11-20 | 0000-00-00 | No | No | Current |
| 0472-0094-75 | 00472009475 | 2 BOTTLE, DROPPER in 1 CARTON (0472-0094-75) > 60 mL in 1 BOTTLE, DROPPER | 2000-11-20 | 0000-00-00 | No | No | Current |