MINOXIDIL
- Product NDC
- 63629-1084
- 11-digit product format
- 636291084
- Labeler code
- 63629
- Product ID
- 63629-1084_ce37c26a-c761-4189-9439-d33039b73bfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072709
- Marketing category
- ANDA
- Marketing start
- 2020-07-05
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 3 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1084-1 | 63629108401 | 100 TABLET in 1 BOTTLE (63629-1084-1) | 100 tablet | 2020-07-05 | 0000-00-00 | No | No | Current |