NDC 61919-732

Losartan Potassium HCTZ

Losartan Potassium Hctz

Losartan Potassium HCTZ is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Hydrochlorothiazide; Losartan Potassium.

Product ID61919-732_86cecd00-526b-60b6-e053-2991aa0a2d29
NDC61919-732
Product TypeHuman Prescription Drug
Proprietary NameLosartan Potassium HCTZ
Generic NameLosartan Potassium Hctz
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-04-18
Marketing CategoryANDA / ANDA
Application NumberANDA091629
Labeler NameDIRECT RX
Substance NameHYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Active Ingredient Strength13 mg/1; mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 61919-732-90

90 TABLET, FILM COATED in 1 BOTTLE (61919-732-90)
Marketing Start Date2019-04-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61919-732-90 [61919073290]

Losartan Potassium HCTZ TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-18

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE12.5 mg/1

OpenFDA Data

SPL SET ID:982c6ccb-f0b2-4e77-8e05-d9f821300740
Manufacturer
UNII

Pharmacological Class

  • Increased Diuresis [PE]
  • Thiazide Diuretic [EPC]
  • Thiazides [CS]
  • Angiotensin 2 Receptor Antagonists [MoA]
  • Angiotensin 2 Receptor Blocker [EPC]

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