MINOXIDIL
- Product NDC
- 70518-3419
- 11-digit product format
- 705183419
- Labeler code
- 70518
- Product ID
- 70518-3419_df34797a-d0a9-4232-e053-2a95a90af7b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072709
- Marketing category
- ANDA
- Marketing start
- 2022-05-15
- 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
- 2023-12-31
- 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 |
|---|
| 70518-3419-0 | 70518341900 | 100 POUCH in 1 BOX (70518-3419-0) > 1 TABLET in 1 POUCH (70518-3419-1) | 100 pouch | 2022-05-15 | 0000-00-00 | No | No | Current |