NDC 70954-959 – Methenamine Hippurate

Methenamine Hippurate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC70954-959

Product details

Brand name
Methenamine Hippurate
Generic name
Methenamine Hippurate
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA017681
Marketed since
July 27, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Methenamine Hippurate →

Package NDC codes (1)

Package NDCDescriptionSince
70954-959-10100 TABLET in 1 BOTTLE (70954-959-10)Jul 27, 2026

Other Methenamine Hippurate products