Minoxidil
- Product NDC
- 56062-798
- 11-digit product format
- 560620798
- Labeler code
- 56062
- Product ID
- 56062-798_994c849a-a30c-473b-87fd-ce7fc9a0a535
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Publix Super Markets Inc
- Application
- ANDA075598
- Marketing category
- ANDA
- Marketing start
- 2010-10-25
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 3 g/60mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56062-798 | MINOXIDIL SOLUTION [PUBLIX SUPER MARKETS INC] | 4 | Legacy NDC | 20210806_0b822988-2d8c-4e16-aafd-6058008c0910.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56062-798-16 | 56062079816 | 1 BOTTLE in 1 CARTON (56062-798-16) > 60 mL in 1 BOTTLE | 1 bottle | 2010-10-25 | 0000-00-00 | No | No | Current |