Minoxidil
- Product NDC
- 63629-9433
- 11-digit product format
- 636299433
- Labeler code
- 63629
- Product ID
- 63629-9433_a26e8aa9-523a-41ff-8f24-07845bbbcc0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071826
- Marketing category
- ANDA
- Marketing start
- 1988-11-14
- Substance
- MINOXIDIL
- Active strength
- 2.5 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 | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 197987 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-9433-1 | Minoxidil | 30 in 1 BOTTLE | TABLET | 30 | | 104 |
| 63629-9433-2 | Minoxidil | 90 in 1 BOTTLE | TABLET | 90 | | 104 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-9433 | MINOXIDIL TABLET [BRYANT RANCH PREPACK] | 104 | Current NDC, Legacy NDC, 2 package rows | 20240524_75b2832c-0a6c-4125-9514-19a6d8dbf6cf.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 |
|---|
| 63629-9433-1 | 63629943301 | 30 TABLET in 1 BOTTLE (63629-9433-1) | 30 tablet | 2022-10-05 | 0000-00-00 | No | No | Current |
| 63629-9433-2 | 63629943302 | 90 TABLET in 1 BOTTLE (63629-9433-2) | 90 tablet | 2024-02-23 | | No | No | Current |