Folic Acid
- Product NDC
- 71335-2849
- 11-digit product format
- 713352849
- Labeler code
- 71335
- Product ID
- 71335-2849_588a56ed-e8d0-48b3-84ff-db18a211fa1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211064
- Marketing category
- ANDA
- Marketing start
- 2018-02-09
- 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#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2849-1 | 71335284901 | 30 TABLET in 1 BOTTLE (71335-2849-1) | 30 tablet | 2025-10-22 | No | No | Current |
| 71335-2849-2 | 71335284902 | 100 TABLET in 1 BOTTLE (71335-2849-2) | 100 tablet | 2025-10-22 | No | No | Current |
| 71335-2849-3 | 71335284903 | 120 TABLET in 1 BOTTLE (71335-2849-3) | 120 tablet | 2025-10-22 | No | No | Current |
| 71335-2849-4 | 71335284904 | 50 TABLET in 1 BOTTLE (71335-2849-4) | 50 tablet | 2025-10-22 | No | No | Current |
| 71335-2849-5 | 71335284905 | 90 TABLET in 1 BOTTLE (71335-2849-5) | 90 tablet | 2025-10-22 | No | No | Current |
| 71335-2849-6 | 71335284906 | 60 TABLET in 1 BOTTLE (71335-2849-6) | 60 tablet | 2025-10-22 | No | No | Current |
| 71335-2849-7 | 71335284907 | 10 TABLET in 1 BOTTLE (71335-2849-7) | 10 tablet | 2025-10-22 | No | No | Current |