NDC 60687-694

Methenamine Hippurate

Methenamine Hippurate

Methenamine Hippurate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by American Health Packaging. The primary component is Methenamine Hippurate.

Product ID60687-694_e468ecf1-aa68-132d-e053-2a95a90afd0c
NDC60687-694
Product TypeHuman Prescription Drug
Proprietary NameMethenamine Hippurate
Generic NameMethenamine Hippurate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-07-20
Marketing CategoryANDA /
Application NumberANDA212172
Labeler NameAmerican Health Packaging
Substance NameMETHENAMINE HIPPURATE
Active Ingredient Strength1000 mg/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 60687-694-21

30 BLISTER PACK in 1 CARTON (60687-694-21) > 1 TABLET in 1 BLISTER PACK (60687-694-11)
Marketing Start Date2022-07-20
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Methenamine Hippurate" or generic name "Methenamine Hippurate"

NDCBrand NameGeneric Name
0115-1754Methenamine HippurateMethenamine Hippurate
0955-1037Methenamine HippurateMethenamine Hippurate
42571-332Methenamine HippurateMethenamine Hippurate
43199-020Methenamine HippurateMethenamine Hippurate
47781-577Methenamine HippurateMethenamine Hippurate
50268-549Methenamine HippurateMethenamine Hippurate
50742-142METHENAMINE HIPPURATEmethenamine hippurate
60687-694Methenamine HippurateMethenamine Hippurate
64720-139Methenamine HippurateMethenamine Hippurate
65862-782Methenamine HippurateMethenamine Hippurate
68151-0984Methenamine HippurateMethenamine Hippurate
69315-210Methenamine HippurateMethenamine Hippurate
30698-277HIPREXMethenamine Hippurate
30698-477HIPREXMethenamine Hippurate

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.