FOLIC ACID
- Product NDC
- 72162-2557
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- folic acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204418
- Marketing category
- ANDA
- Substance
- FOLIC ACID
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2557-0 | 1000 TABLET in 1 BOTTLE (72162-2557-0) | 2025-10-21 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Folic Acid Tablets, USP | Bryant Ranch Prepack | 2025-10-21 | HUMAN PRESCRIPTION DRUG LABEL | 100 |