Folic Acid
- Product NDC
- 63739-110
- 11-digit product format
- 637390110
- Labeler code
- 63739
- Product ID
- 63739-110_144ee59e-bf4b-462d-8b67-3863836e36ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Packaging Services Business Unit of McKesson Corporation.
- Application
- ANDA080600
- Marketing category
- ANDA
- Marketing start
- 2004-11-24
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#