FOLIC ACID
- Product NDC
- 72162-2557
- 11-digit product format
- 721622557
- Labeler code
- 72162
- Product ID
- 72162-2557_40705e87-44f9-4cc4-a5d3-5b897b00664a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- folic acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 72162-2557-0 | FOLIC ACID | 1000 in 1 BOTTLE | TABLET | 1000 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2557-0 | 72162255700 | 1000 TABLET in 1 BOTTLE (72162-2557-0) | 1000 tablet | 2025-10-21 | No | No | Current |