Folic acid
- Product NDC
- 68071-2204
- 11-digit product format
- 680712204
- Labeler code
- 68071
- Product ID
- 68071-2204_d738dd07-6927-9325-e053-2995a90a026d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090035
- Marketing category
- ANDA
- Marketing start
- 2019-05-30
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2204-1 | 68071220401 | 100 TABLET in 1 BOTTLE (68071-2204-1) | 100 tablet | 2020-06-30 | 0000-00-00 | No | No | Current |