NDC 69367-436 – Methenamine Mandelate

Methenamine Mandelate 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC69367-436

Product details

Brand name
Methenamine Mandelate
Generic name
Methenamine Mandelate
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
March 19, 2026
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
69367-436-01100 TABLET, FILM COATED in 1 BOTTLE (69367-436-01)Mar 19, 2026
69367-436-6060 TABLET, FILM COATED in 1 BOTTLE (69367-436-60)Mar 19, 2026

Other Methenamine Mandelate products