# Betaine Anhydrous

NDC: 71863-115
Generic name: Betaine Anhydrous
Labeler / Manufacturer: Eton Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20220128

FDA application: ANDA210508

## Active ingredients

- BETAINE: 1 g/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71863-115"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71863-115
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee8a95c3-df9f-6e55-e053-2a95a90ab17b