FOLIC ACID
- Product NDC
- 43063-791
- 11-digit product format
- 430630791
- Labeler code
- 43063
- Product ID
- 43063-791_303d4c3e-cdbc-1691-e063-6294a90ac6d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- folic acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA204418
- Marketing category
- ANDA
- Marketing start
- 2015-08-04
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FOLIC ACID
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FOLIC ACID | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 935E97BOY8 |
| Rxcui | 310410 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43063-791-30 | FOLIC ACID | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 13 |
| 43063-791-90 | FOLIC ACID | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-791 | FOLIC ACID TABLET [PD-RX PHARMACEUTICALS, INC.] | 13 | Current NDC, Legacy NDC, 2 package rows | 20250316_726bb436-69e3-452f-9f28-153b58bf3ca5.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 |
|---|
| 43063-791-30 | 43063079130 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-791-30) | 30 tablet | 2017-10-02 | 0000-00-00 | No | No | Current |
| 43063-791-90 | 43063079190 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-791-90) | 90 tablet | 2017-10-18 | 0000-00-00 | No | No | Current |