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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 935E97BOY8 | FOLIC ACID | 59-30-3 | FOLIC ACID |
Packages
| 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 | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Folic Acid | Bryant Ranch Prepack | 2025-10-29 | HUMAN PRESCRIPTION DRUG LABEL | 100 |