Follinique
- Product NDC
- 70788-579
- 11-digit product format
- 707880579
- Labeler code
- 70788
- Product ID
- 70788-579_0622cd54-1f64-4193-88db-eae3f84658b9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Premium Distribution, LLC
- Application
- ANDA078176
- Marketing category
- ANDA
- Marketing start
- 2016-10-27
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 20 mg/mL
- 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 |
|---|
| 70788-579-01 | Follinique | 60 mL in 1 BOTTLE, DROPPER | SOLUTION | 60 | | 1 |
| 70788-579-01 | Follinique | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70788-579 | FOLLINIQUE (MINOXIDIL) SOLUTION [PREMIUM DISTRIBUTION, LLC] | 1 | Legacy NDC, 2 package rows | 20170428_e90a949e-e200-46d5-ae3b-b4f47f3fe022.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70788-579-01 | 70788057901 | 60 mL in 1 BOTTLE, DROPPER | 60 ml | Historical |