# FOLIC ACID

NDC: 11534-165
Generic name: folic acid
Labeler / Manufacturer: SUNRISE PHARMACEUTICAL, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150804

FDA application: ANDA204418

## Active ingredients

- FOLIC ACID: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11534-165"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11534-165
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6854412b-7ecb-4107-85eb-730f14e23f06