minoxidil
- Product NDC
- 56062-070
- 11-digit product format
- 560620070
- Labeler code
- 56062
- Product ID
- 56062-070_2bd3521f-19bd-4f77-9034-9ae287698992
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Publix Super Markets Inc
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2021-12-16
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- minoxidil
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 2 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 311723 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56062-070-16 | minoxidil | 60 mL in 1 BOTTLE, DROPPER | SOLUTION | 60 | | 3 |
| 56062-070-16 | minoxidil | 1 in 1 CARTON | SOLUTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56062-070 | MINOXIDIL SOLUTION [PUBLIX SUPER MARKETS INC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20221118_d0ff44ef-d59c-43c9-a381-448fef2cfe22.zip |
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 |
|---|
| 56062-070-16 | 56062007016 | 1 BOTTLE, DROPPER in 1 CARTON (56062-070-16) / 60 mL in 1 BOTTLE, DROPPER | 2021-12-16 | 0000-00-00 | No | No | Current |