Nioxin Hair Regrowth Treatment for Women
- Product NDC
- 69282-001
- 11-digit product format
- 692820001
- Labeler code
- 69282
- Product ID
- 69282-001_d62281d9-1864-06f4-e053-2a95a90a1128
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- The Wella Corporation
- Application
- ANDA075357
- Marketing category
- ANDA
- Marketing start
- 2014-11-01
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69282-001-18 | 69282000118 | 3 BOTTLE, DROPPER in 1 CARTON (69282-001-18) > 60 mL in 1 BOTTLE, DROPPER | 2014-11-01 | 0000-00-00 | No | No | Current |
| 69282-001-60 | 69282000160 | 1 BOTTLE, DROPPER in 1 CARTON (69282-001-60) > 60 mL in 1 BOTTLE, DROPPER | 2014-11-01 | 0000-00-00 | No | No | Current |