Minoxidil
- Product NDC
- 68151-2032
- 11-digit product format
- 681512032
- Labeler code
- 68151
- Product ID
- 68151-2032_d752129d-78a3-4d36-855e-41b42a7c721e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA071345
- Marketing category
- ANDA
- Marketing start
- 2009-10-26
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-2032-7 | Minoxidil | 1 in 1 CUP, UNIT-DOSE | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2032 | MINOXIDIL TABLET [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20160311_9a290e8e-730a-4160-a367-c003bc04a2aa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2032-7 | 68151203207 | 1 in 1 CUP, UNIT-DOSE | Historical |