NDC 61919-873

LOSARTAN POT/HCTZ

Losartan Pot/hctz

LOSARTAN POT/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 Losartan Potassium; Hydrochlorothiazide.

• Product ID: 61919-873_8a99337b-ac20-27c2-e053-2a95a90a4bd6
• NDC: 61919-873
• Product Type: Human Prescription Drug
• Proprietary Name: LOSARTAN POT/HCTZ
• Generic Name: Losartan Pot/hctz
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2019-06-05
• Marketing Category: ANDA / ANDA
• Application Number: ANDA091629
• Labeler Name: Direct_Rx
• Substance Name: LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
• Active Ingredient Strength: 100 mg/1; mg/1
• Pharm Classes: Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 61919-873-90

90 TABLET, FILM COATED in 1 BOTTLE (61919-873-90)

• Marketing Start Date: 2019-06-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61919-873-90 [61919087390]

LOSARTAN POT/HCTZ TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA091629
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-06-05

Drug Details

Active Ingredients

Ingredient	Strength
LOSARTAN POTASSIUM	100 mg/1

OpenFDA Data

• SPL SET ID: 8a99337b-ac1f-27c2-e053-2a95a90a4bd6
• Manufacturer:
  • Direct_Rx
• UNII:
  • 3ST302B24A
  • 0J48LPH2TH

Pharmacological Class

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