Regenpure Precision
- Product NDC
- 71290-813
- 11-digit product format
- 712900813
- Labeler code
- 71290
- Product ID
- 71290-813_4a116d5a-332b-68b6-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MINOXIDIL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Salonceuticals, Inc.
- Application
- ANDA076239
- Marketing category
- ANDA
- Marketing start
- 2017-03-04
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Regenpure Precision
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 311724 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71290-813-02 | Regenpure Precision | 1 in 1 BOX | LIQUID | 1 | | 1 |
| 71290-813-02 | Regenpure Precision | 60 mL in 1 BOTTLE | LIQUID | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71290-813 | REGENPURE PRECISION (MINOXIDIL) LIQUID [SALONCEUTICALS, INC.] | 1 | Current NDC, Legacy NDC, 2 package rows | 20170306_4a113921-b2a9-42cc-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71290-813-02 | 71290081302 | 1 BOTTLE in 1 BOX (71290-813-02) / 60 mL in 1 BOTTLE | 1 bottle | 2017-03-05 | 0000-00-00 | No | No | Current |