Minoxidil
- Product NDC
- 0472-0066
- 11-digit product format
- 004720066
- Labeler code
- 0472
- Product ID
- 0472-0066_bae3e6a5-32b5-4dd3-a6f3-c33ca814ce34
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA074588
- Marketing category
- ANDA
- Marketing start
- 1996-04-05
- 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 RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0472-0066-73 | 00472006673 | 1 BOTTLE, DROPPER in 1 CARTON (0472-0066-73) > 60 mL in 1 BOTTLE, DROPPER | 1996-04-05 | 0000-00-00 | No | No | Current |
| 0472-0066-75 | 00472006675 | 2 BOTTLE, DROPPER in 1 CARTON (0472-0066-75) > 60 mL in 1 BOTTLE, DROPPER | 1996-04-05 | 0000-00-00 | No | No | Current |