Folic Acid
- Product NDC
- 71335-2858
- 11-digit product format
- 713352858
- Labeler code
- 71335
- Product ID
- 71335-2858_4252bf12-4682-253b-e063-6394a90a6b90
- 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#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2858-1 | 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 |
|---|
| 71335-2858-1 | 71335285801 | 1000 TABLET in 1 BOTTLE (71335-2858-1) | 1000 tablet | 2025-10-29 | No | No | Current |