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NDC 62135-0200-01 Methenamine Mandelate 500 mg/1 Details

Methenamine Mandelate 500 mg/1

Methenamine Mandelate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is METHENAMINE MANDELATE.

MedlinePlus Drug Summary

Methenamine, an antibiotic, eliminates bacteria that cause urinary tract infections. It usually is used on a long-term basis to treat chronic infections and to prevent recurrence of infections. Antibiotics will not work for colds, flu, or other viral infections. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 62135-0200-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Methenamine

Product Information

NDC	62135-0200
Product ID	62135-200_00225fc8-eb0d-a4cc-e063-6394a90a2acb
Associated GPIs	16800020100310
GCN Sequence Number	009462
GCN Sequence Number Description	methenamine mandelate TABLET 500 MG ORAL
HIC3	W2G
HIC3 Description	ANTIBIOTIC, ANTIBACTERIAL, MISC.
GCN	42036
HICL Sequence Number	004102
HICL Sequence Number Description	METHENAMINE MANDELATE
Brand/Generic	Generic
Proprietary Name	Methenamine Mandelate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Methenamine Mandelate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	METHENAMINE MANDELATE
Labeler Name	Chartwell RX, LLC
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2024-12-31

Package

NDC 62135-0200-01 (62135020001)

Pricing Information	N/A
NDC Package Code	62135-200-01
Billing NDC	62135020001
Package	100 TABLET, FILM COATED in 1 BOTTLE (62135-200-01)
Marketing Start Date	2021-10-01
NDC Exclude Flag	N