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NDC 62135-0201-01 Methenamine Mandelate 1000 mg/1 Details

Methenamine Mandelate 1000 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: 62135-0201-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Methenamine

Product Information

NDC	62135-0201
Product ID	62135-201_00225fc8-eb0d-a4cc-e063-6394a90a2acb
Associated GPIs	16800020100320
GCN Sequence Number	009460
GCN Sequence Number Description	methenamine mandelate TABLET 1 G ORAL
HIC3	W2G
HIC3 Description	ANTIBIOTIC, ANTIBACTERIAL, MISC.
GCN	42032
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	1000
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 62135-0201-01 (62135020101)

Pricing Information	N/A
NDC Package Code	62135-201-01
Billing NDC	62135020101
Package	100 TABLET, FILM COATED in 1 BOTTLE (62135-201-01)
Marketing Start Date	2021-10-01
NDC Exclude Flag	N