United States · FDA National Drug Code directory
Betaine Anhydrous
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71863-115_42c7a42b-6a75-69d3-e063-6294a90acc18
- Product NDC
- 71863-115
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Betaine Anhydrous
- Labeler
- Eton Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220128
- Source listing expiry
- 20261231
Source-listed ingredients
- BETAINE — 1 g/g
These values do not establish equivalence or a dose recommendation.
Packages
- 180 g in 1 BOTTLE (71863-115-18) · 71863-115-18
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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