NDC 72789-030

Furosemide

Furosemide

Furosemide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pd-rx Pharmaceuticals, Inc.. The primary component is Furosemide.

Product ID72789-030_9947a3a6-0302-093e-e053-2a95a90adbbe
NDC72789-030
Product TypeHuman Prescription Drug
Proprietary NameFurosemide
Generic NameFurosemide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2004-03-26
Marketing CategoryANDA / ANDA
Application NumberANDA076796
Labeler NamePD-Rx Pharmaceuticals, Inc.
Substance NameFUROSEMIDE
Active Ingredient Strength20 mg/1
Pharm ClassesIncreased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72789-030-30

30 TABLET in 1 BOTTLE, PLASTIC (72789-030-30)
Marketing Start Date2019-12-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72789-030-30 [72789003030]

Furosemide TABLET
Marketing CategoryANDA
Application NumberANDA076796
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-12-05

NDC 72789-030-60 [72789003060]

Furosemide TABLET
Marketing CategoryANDA
Application NumberANDA076796
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-12-05

Drug Details

Active Ingredients

IngredientStrength
FUROSEMIDE20 mg/1

Pharmacological Class

  • Increased Diuresis at Loop of Henle [PE]
  • Loop Diuretic [EPC]
  • Increased Diuresis at Loop of Henle [PE]
  • Loop Diuretic [EPC]

NDC Crossover Matching brand name "Furosemide" or generic name "Furosemide"

NDCBrand NameGeneric Name
0054-3294FurosemideFurosemide
0054-3298FurosemideFurosemide
0054-4297FurosemideFurosemide
0054-4299FurosemideFurosemide
0054-4301FurosemideFurosemide
0054-8297FurosemideFurosemide
0054-8299FurosemideFurosemide
0054-8301FurosemideFurosemide
0378-0208Furosemidefurosemide
0378-0216Furosemidefurosemide
0378-0232Furosemidefurosemide
0404-9861FurosemideFurosemide
0404-9862FUROSEMIDEfurosemide
0404-9863FurosemideFurosemide
0404-9864FUROSEMIDEfurosemide
0409-1639FurosemideFUROSEMIDE
0409-6102FUROSEMIDEFUROSEMIDE
68071-1708FurosemideFurosemide
68071-1809FurosemideFurosemide
68071-3273FurosemideFurosemide
68071-3144FurosemideFurosemide
68071-3194FurosemideFurosemide
68071-3148FurosemideFurosemide
68071-4015FurosemideFurosemide
68071-4022FurosemideFurosemide
68071-4349FurosemideFurosemide
68071-4534FurosemideFurosemide
0409-9631FurosemideFurosemide
68071-4445FurosemideFurosemide
68071-4522FurosemideFurosemide
68094-867FurosemideFurosemide
68094-756FurosemideFurosemide
68788-1966FurosemideFurosemide
68788-6397FurosemideFurosemide
68788-6784FurosemideFurosemide
68788-7265FurosemideFurosemide
68788-6948FurosemideFurosemide
68788-9226FurosemideFurosemide
68788-7354FurosemideFurosemide
68788-9778FurosemideFurosemide
69315-116FurosemideFurosemide
69315-118FurosemideFurosemide
69315-117FurosemideFurosemide
69677-204FurosemideFurosemide
70121-1164FurosemideFurosemide
70121-1076FurosemideFurosemide
70121-1163FurosemideFurosemide
70518-0092FurosemideFurosemide
70518-0584FurosemideFurosemide
70518-0120FurosemideFurosemide

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