FOLIC ACID
- Product NDC
- 55700-698
- 11-digit product format
- 557000698
- Labeler code
- 55700
- Product ID
- 55700-698_4b114cd3-eb38-4f08-86da-8dceaf611a99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FOLIC ACID
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA040796
- Marketing category
- ANDA
- Marketing start
- 2018-11-02
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55700-698-30 | EA - Each | 55700-698 | bb243fe3-21d0-4a33-9301-7ed279d32c8f | 1 | 2018-12-13 |