minoxidil
- Product NDC
- 0472-1665
- 11-digit product format
- 004721665
- Labeler code
- 0472
- Product ID
- 0472-1665_53ac6d62-055d-4959-a6b9-8e73627f16d5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA208092
- Marketing category
- ANDA
- Marketing start
- 2017-12-29
- Marketing end
- 2021-12-31
- Substance
- MINOXIDIL
- Active strength
- 5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0472-1665-85 | 00472166585 | 1 CAN in 1 CAPSULE (0472-1665-85) > 60 g in 1 CAN | 1 can | 2017-12-29 | 2021-12-31 | No | No | Current |
| 0472-1665-87 | 00472166587 | 2 CAN in 1 CARTON (0472-1665-87) > 60 g in 1 CAN | 2 can | 2017-12-29 | 2021-12-31 | No | No | Current |