losartan potassium

Generic: losartan potassium

Labeler: aiping pharmaceutical, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler aiping pharmaceutical, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
AiPing Pharmaceutical, Inc.

Identifiers & Regulatory

Product NDC 11788-101
Product ID 11788-101_0768a3af-f3b0-406b-bedb-c4c4bf11d1d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090544
Listing Expiration 2026-12-31
Marketing Start 2025-12-15

Pharmacologic Class

Classes
angiotensin 2 receptor antagonists [moa] angiotensin 2 receptor blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11788101
Hyphenated Format 11788-101

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0311788101309 0311788100906 0311788101903
UNII
3ST302B24A

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name losartan potassium (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA090544 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (11788-101-10)
  • 30 TABLET in 1 BOTTLE (11788-101-30)
  • 90 TABLET in 1 BOTTLE (11788-101-90)
source: ndc

Packages (3)

11788-101-10 1000 TABLET in 1 BOTTLE (11788-101-10) 11788-101-30 30 TABLET in 1 BOTTLE (11788-101-30) 11788-101-90 90 TABLET in 1 BOTTLE (11788-101-90)

Ingredients (1)

losartan potassium (50 mg/1)

Linked Drug Pages (1)

Losartan Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0768a3af-f3b0-406b-bedb-c4c4bf11d1d4", "openfda": {"upc": ["0311788101309", "0311788100906", "0311788101903"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["1ae817aa-5221-4387-a457-306785140741"], "manufacturer_name": ["AiPing Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (11788-101-10)", "package_ndc": "11788-101-10", "marketing_start_date": "20251215"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (11788-101-30)", "package_ndc": "11788-101-30", "marketing_start_date": "20251215"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (11788-101-90)", "package_ndc": "11788-101-90", "marketing_start_date": "20251215"}], "brand_name": "Losartan Potassium", "product_id": "11788-101_0768a3af-f3b0-406b-bedb-c4c4bf11d1d4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "11788-101", "generic_name": "Losartan Potassium", "labeler_name": "AiPing Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090544", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}