MINOXIDIL
- Product NDC
- 63629-1086
- 11-digit product format
- 636291086
- Labeler code
- 63629
- Product ID
- 63629-1086_236dceaa-cec4-48ef-91b5-3371e3d92d87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072709
- Marketing category
- ANDA
- Marketing start
- 1995-12-14
- Substance
- MINOXIDIL
- Active strength
- 10 mg/1
- 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 197986 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-1086-1 | MINOXIDIL | 100 in 1 BOTTLE | TABLET | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-1086 | MINOXIDIL TABLET [BRYANT RANCH PREPACK] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240110_40da3ec5-39db-42f1-b0d6-39d852130307.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 |
|---|
| 63629-1086-1 | 63629108601 | 100 TABLET in 1 BOTTLE (63629-1086-1) | 100 tablet | 1995-12-14 | 0000-00-00 | No | No | Current |