Folic Acid
- Product NDC
- 60687-681
- 11-digit product format
- 606870681
- Labeler code
- 60687
- Product ID
- 60687-681_437e6d15-c5e5-2c06-e063-6394a90a59cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA040625
- Marketing category
- ANDA
- Marketing start
- 2022-07-15
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 60687-681-01 | 60687068101 | 100 BLISTER PACK in 1 CARTON (60687-681-01) / 1 TABLET in 1 BLISTER PACK (60687-681-11) | 100 blister pack | 2022-07-15 | No | No | Historical |