NDC 62135-200 – Methenamine Mandelate

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

Human Prescription Drug

Product NDC62135-200

Product details

Brand name
Methenamine Mandelate
Generic name
Methenamine Mandelate
Labeler
Chartwell RX, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
October 1, 2021
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
62135-200-01100 TABLET, FILM COATED in 1 BOTTLE (62135-200-01)Oct 1, 2021
62135-200-12120 TABLET, FILM COATED in 1 BOTTLE (62135-200-12)Oct 1, 2021
62135-200-6060 TABLET, FILM COATED in 1 BOTTLE (62135-200-60)Oct 1, 2021

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