Home Applications 016151 Application 016151
Type NDA
Sponsor CNTY LINE PHARMS Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 UREX METHENAMINE HIPPURATE TABLET;ORAL 1GM No No
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N016151-001 UREX METHENAMINE HIPPURATE 1GM TABLET / ORAL AB Approved before 1982
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code N016151-001 AB
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 2 of 2 · 43 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2022-09-29 23:25 UTC 2022-09 N016151-001 UREX 1GM TABLET / ORAL AB Approved before 1982 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 N016151-001 UREX 1GM TABLET / ORAL AB Approved before 1982 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N016151-001 UREX 1GM TABLET / ORAL AB Approved before 1982 a50c72e98297…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 43 observed states.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
NDC Listings For This Application# NDC listings for this application page 1 of 1 · 6 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 43199-020 Methenamine Hippurate Methenamine Hippurate County Line Pharmaceuticals, LLC NDA Current 47781-577 Methenamine Hippurate Methenamine Hippurate Alvogen Inc. NDA Current 47781-577 Methenamine Hippurate Methenamine Hippurate Alvogen Inc. NDA Current 47781-577 Methenamine Hippurate Methenamine Hippurate Alvogen Inc. NDA Current 47781-577 Methenamine Hippurate Methenamine Hippurate Alvogen Inc. NDA Current 47781-577 Methenamine Hippurate Methenamine Hippurate Alvogen Inc. NDA Current
Documents# Document, Submission type, Date table Document Submission type Date 33147 SUPPL 2008-03-13 12977 SUPPL 2008-03-13