NDC 71863-115 – Betaine Anhydrous

Betaine 1 g/g · Powder, For Solution · Oral

Human Prescription Drug

Product NDC71863-115

Product details

Brand name
Betaine Anhydrous
Generic name
Betaine Anhydrous
Labeler
Eton Pharmaceuticals, Inc.
Dosage form
Powder, For Solution
Route
Oral
Marketing category
ANDA · ANDA210508
Marketed since
January 28, 2022
Listing expires
December 31, 2026
Pharmacologic class
Methylating Agent

Active ingredients

Uses, dosage, side effects and warnings for Betaine Anhydrous →

Package NDC codes (1)

Package NDCDescriptionSince
71863-115-18180 g in 1 BOTTLE (71863-115-18)Jan 28, 2022