Folic acid
- Product NDC
- 68788-7624
- 11-digit product format
- 687887624
- Labeler code
- 68788
- Product ID
- 68788-7624_07445889-99ed-48da-a044-ddb14efb5cfb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090035
- Marketing category
- ANDA
- Marketing start
- 2020-03-06
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7624-3 | 68788762403 | 30 TABLET in 1 BOTTLE (68788-7624-3) | 30 tablet | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7624-6 | 68788762406 | 60 TABLET in 1 BOTTLE (68788-7624-6) | 60 tablet | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7624-9 | 68788762409 | 90 TABLET in 1 BOTTLE (68788-7624-9) | 90 tablet | 2020-03-06 | 0000-00-00 | No | No | Current |