minoxidil
- Product NDC
- 11822-0702
- 11-digit product format
- 118220702
- Labeler code
- 11822
- Product ID
- 11822-0702_5968744f-4812-4ba8-ad8e-5cf839673deb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2022-03-07
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- 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 |
|---|
| 11822-0702-1 | 11822070201 | 3 BOTTLE in 1 CARTON (11822-0702-1) > 60 mL in 1 BOTTLE | 3 bottle | 2022-03-07 | 0000-00-00 | No | No | Current |