minoxidil
- Product NDC
- 56062-202
- 11-digit product format
- 560620202
- Labeler code
- 56062
- Product ID
- 56062-202_4a14695d-3713-4a66-a9cd-20d9e1f955e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Publix Super Markets Inc
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2011-04-04
- 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 Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56062-202 | MINOXIDIL FOR WOMEN (MINOXIDIL) SOLUTION [PUBLIX SUPER MARKETS INC] | 6 | Legacy NDC | 20210921_477cdc2c-4e4f-47ed-80b8-b7d9729bb587.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56062-202-16 | 56062020216 | 1 BOTTLE in 1 CARTON (56062-202-16) > 60 mL in 1 BOTTLE | 1 bottle | 2011-04-04 | 0000-00-00 | No | No | Current |