Betaine Anhydrous
NDC 71863-115, Betaine Anhydrous, powder, for solution, from Eton Pharmaceuticals, Inc..
- Product NDC
- 71863-115
- Status
- Listed
- Labeler
- Eton Pharmaceuticals, Inc.
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210508
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71863-115 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BETAINE1 g/g
Pharmacologic classes
Methylating Activity [MoA]; Methylating Agent [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71863-115-18 | 71863011518 | 180 g in 1 BOTTLE (71863-115-18) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/ee8a95c3-df9f-6e55-e053-2a95a90ab17b
Use it
Look up 71863-115 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71863-115 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71863-115. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.