NDC 69543-141

Losartan

Losartan Potassium

Losartan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Virtus Pharmaceuticals. The primary component is Losartan Potassium.

• Product ID: 69543-141_52f7a69e-4d34-4be4-81ab-8674bd0958e8
• NDC: 69543-141
• Product Type: Human Prescription Drug
• Proprietary Name: Losartan
• Generic Name: Losartan Potassium
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2015-07-14
• Marketing End Date: 2019-05-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA090382
• Labeler Name: Virtus Pharmaceuticals
• Substance Name: LOSARTAN POTASSIUM
• Active Ingredient Strength: 50 mg/1
• Pharm Classes: Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
• NDC Exclude Flag: N

Packaging

NDC 69543-141-11

1000 TABLET, FILM COATED in 1 BOTTLE (69543-141-11)

• Marketing Start Date: 2015-07-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69543-141-11 [69543014111]

Losartan TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090382
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-07-14
• Marketing End Date: 2019-05-30

NDC 69543-141-30 [69543014130]

Losartan TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090382
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-07-14
• Marketing End Date: 2019-05-30

NDC 69543-141-10 [69543014110]

Losartan TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090382
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2015-07-14
• Marketing End Date: 2015-07-14

NDC 69543-141-90 [69543014190]

Losartan TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090382
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-07-14
• Marketing End Date: 2019-05-30

Drug Details

Active Ingredients

Ingredient	Strength
LOSARTAN POTASSIUM	50 mg/1

OpenFDA Data

• SPL SET ID: a98a821c-7b81-4f9b-9801-1a16d71871ce
• Manufacturer:
  • Virtus Pharmaceuticals
• UNII:
  • 3ST302B24A
• RxNorm Concept Unique ID - RxCUI:
  • 979485
  • 979492
  • 979480
• UPC Code:
  • 0369543141305
  • 0369543142302
  • 0369543140308

Pharmacological Class

• Angiotensin 2 Receptor Antagonists [MoA]
• Angiotensin 2 Receptor Blocker [EPC]

Medicade Reported Pricing

69543014190 LOSARTAN POTASSIUM 50 MG TAB

Pricing Unit: EA | Drug Type:

69543014130 LOSARTAN POTASSIUM 50 MG TAB

Pricing Unit: EA | Drug Type:

69543014111 LOSARTAN POTASSIUM 50 MG TAB

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Losartan" or generic name "Losartan Potassium"

NDC	Brand Name	Generic Name
69543-141	Losartan	Losartan
50090-2908	Losartan	Losartan
0006-0951	COZAAR	losartan potassium
0006-0952	COZAAR	losartan potassium
0006-0960	COZAAR	losartan potassium
0054-0123	Losartan Potassium	Losartan Potassium
0054-0124	Losartan Potassium	Losartan Potassium
0054-0125	Losartan Potassium	Losartan Potassium
0093-7364	Losartan Potassium	Losartan Potassium
0093-7365	Losartan Potassium	Losartan Potassium
0093-7366	Losartan Potassium	Losartan Potassium
0179-0200	Losartan Potassium	Losartan Potassium
0179-0202	Losartan Potassium	Losartan Potassium
0179-0203	Losartan Potassium	Losartan Potassium
0615-7604	Losartan Potassium	Losartan Potassium
0615-7605	Losartan Potassium	Losartan Potassium
0615-7606	Losartan Potassium	Losartan Potassium
0615-7958	Losartan Potassium	Losartan Potassium
0615-7959	Losartan Potassium	Losartan Potassium
0615-7960	Losartan Potassium	Losartan Potassium
0615-8207	Losartan Potassium	Losartan Potassium
0615-8208	Losartan Potassium	Losartan Potassium
0615-8209	Losartan Potassium	Losartan Potassium
0781-5700	Losartan potassium	losartan potassium
0781-5701	Losartan potassium	losartan potassium
0781-5702	Losartan potassium	losartan potassium