Folixapure
- Product NDC
- 59088-163
- 11-digit product format
- 590880163
- Labeler code
- 59088
- Product ID
- 59088-163_f2048d71-679b-98f8-e053-2995a90a533a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid, Vitamin D3
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-07-10
- Substance
- FOLIC ACID; VITAMIN D
- Active strength
- 1; 125 mg/1; ug/1
- Pharmacologic classes
- Vitamin D [CS], Vitamin D [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Folixapure
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FOLIC ACID | 1 mg/1 |
| VITAMIN D | 125 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 935E97BOY8, 9VU1KI44GP |
| Rxcui | 1720258 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-163-54 | Folixapure | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-163 | FOLIXAPURE (FOLIC ACID, VITAMIN D3) TABLET [PURETEK CORPORATION] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230112_aa1daf3a-9673-6996-e053-2a95a90a5f87.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 |
|---|
| 59088-163-54 | 59088016354 | 30 TABLET in 1 BOTTLE, PLASTIC (59088-163-54) | 30 tablet | 2020-07-10 | 0000-00-00 | No | No | Current |