FOLIC ACID
- Product NDC
- 68071-1800
- 11-digit product format
- 680711800
- Labeler code
- 68071
- Product ID
- 68071-1800_665ca3ab-1a91-0a8f-e053-2a91aa0a1a15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- folic acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA204418
- Marketing category
- ANDA
- Marketing start
- 2015-08-04
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record