minoxidil foam
- Product NDC
- 56062-294
- 11-digit product format
- 560620294
- Labeler code
- 56062
- Product ID
- 56062-294_f73fe89a-cc89-4fac-9e8d-5a13c6d5100b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Publix Super Markets Inc
- Application
- ANDA091344
- Marketing category
- ANDA
- Marketing start
- 2013-06-17
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 5 g/100g
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56062-294-03 | 56062029403 | 3 CAN in 1 CARTON (56062-294-03) > 60 g in 1 CAN | 3 can | 2017-08-30 | 0000-00-00 | No | No | Current |