Methenamine hippurate

Product NDC
70771-1919
11-digit product format
707711919
Labeler code
70771
Product ID
70771-1919_c3524692-fabc-438a-9d6e-2cca27172693
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methenamine hippurate
Dosage form
TABLET
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA219661
Marketing category
ANDA
Marketing start
2025-03-12
Substance
METHENAMINE HIPPURATE
Active strength
1 g/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Methenamine hippurate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METHENAMINE HIPPURATE1 g/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiM329791L57
Rxcui992150

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
260b0da6-d3d7-262f-a60f-d4b36d5f1b4dProduct name620251210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70771-1919-1Methenamine hippurate100 in 1 BOTTLETABLET1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70771-1919METHENAMINE HIPPURATE TABLET [ZYDUS LIFESCIENCES LIMITED]1Current NDC, 1 package rows20250315_7e0d13d1-e564-4f3e-9054-65161eddfc57.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
992150methenamine hippurate 1 GM Oral TabletPSN7e0d13d1-e564-4f3e-9054-65161eddfc571
992150methenamine hippurate 1000 MG Oral TabletSCD7e0d13d1-e564-4f3e-9054-65161eddfc571
992150methenamine hippurate 1 GM Oral TabletSY7e0d13d1-e564-4f3e-9054-65161eddfc571

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70771-1919-170771191901100 TABLET in 1 BOTTLE (70771-1919-1) 100 tablet2025-03-12NoNoCurrent