Methenamine Hippurate

Product NDC
70685-050
11-digit product format
706850050
Labeler code
70685
Product ID
70685-050_d2da3687-6d88-4a79-b6d7-7a0b9b8195f4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methenamine Hippurate
Dosage form
TABLET
Route
ORAL
Labeler
Esjay Pharma LLC
Application
NDA017681
Marketing category
NDA
Marketing start
2025-01-16
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
70685-050-01Methenamine Hippurate100 in 1 BOTTLETABLET1002

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
992150methenamine hippurate 1 GM Oral TabletPSN056b14e1-4e31-4549-880c-4f32cee3516f2
992150methenamine hippurate 1000 MG Oral TabletSCD056b14e1-4e31-4549-880c-4f32cee3516f2
992150methenamine hippurate 1 GM Oral TabletSY056b14e1-4e31-4549-880c-4f32cee3516f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70685-050-0170685005001100 TABLET in 1 BOTTLE (70685-050-01) 100 tablet2025-01-16NoNoHistorical