Folic Acid
- Product NDC
- 70518-3567
- 11-digit product format
- 705183567
- Labeler code
- 70518
- Product ID
- 70518-3567_ec6bb212-c682-6f20-e053-2995a90ab58f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040625
- Marketing category
- ANDA
- Marketing start
- 2022-10-31
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3567-0 | 70518356700 | 30 TABLET in 1 BLISTER PACK (70518-3567-0) | 30 tablet | 2022-10-31 | 0000-00-00 | No | No | Current |