Minoxidil
- Product NDC
- 71713-091
- 11-digit product format
- 717130091
- Labeler code
- 71713
- Product ID
- 71713-091_19f93b56-e00a-42ee-8255-7d47f10fd273
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Thirty MADISON, Inc.
- Application
- ANDA209074
- Marketing category
- ANDA
- Marketing start
- 2022-03-23
- Substance
- MINOXIDIL
- Active strength
- 50 mg/g
- 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
- Brand name suffix
- 5% (For Men)
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 50 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 645146 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71713-091-30 | Minoxidil 5% (For Men) | 3 in 1 CARTON | AEROSOL, FOAM | 3 | | 1 |
| 71713-091-30 | Minoxidil 5% (For Men) | 60 g in 1 CAN | AEROSOL, FOAM | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71713-091 | MINOXIDIL 5% (FOR MEN) (MINOXIDIL) AEROSOL, FOAM [THIRTY MADISON, INC.] | 1 | Current NDC, Legacy NDC, 2 package rows | 20220405_985ba944-147c-4207-b34b-ede702c3d704.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71713-091-30 | 71713009130 | 3 CAN in 1 CARTON (71713-091-30) / 60 g in 1 CAN | 3 can | 2022-03-23 | 0000-00-00 | No | No | Current |