Folic Acid
- Product NDC
- 82804-110
- 11-digit product format
- 828040110
- Labeler code
- 82804
- Product ID
- 82804-110_32203472-8724-4ba7-b0be-d834c3d7f074
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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 |
|---|
| 82804-110-30 | 82804011030 | 30 TABLET in 1 BOTTLE (82804-110-30) | 30 tablet | 2024-06-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Folic Acid | Proficient Rx LP | 2024-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |