losartan potassium (68180-211)

Drug Facts

Product Profile

Brand Name losartan potassium

Generic Name losartan potassium

Labeler lupin pharmaceuticals, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

losartan potassium 50 mg/1

Manufacturer

Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-211

Product ID 68180-211_38431fb6-7157-4be5-929a-0c65b7a29c55

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078232

Listing Expiration 2027-12-31

Marketing Start 2010-10-06

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 68180211

Hyphenated Format 68180-211

Supplemental Identifiers

RxCUI

979480 979485 979492

UPC

0368180212065 0368180376033 0368180210061 0368180378037 0368180308027 0368180376095 0368180211068 0368180309024 0368180377030

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 ANDA078232 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

50 mg/1

source: ndc

Packaging

16 HOW SUPPLIED/STORAGE AND HANDLING Losartan potassium tablet USP is a white film-coated tablet supplied as follows: Losartan Shape Engraving NDC 68180-xxx-xx One side Other side Bottle/90 Bottle/1000 25 mg Capsule shaped LU P21 376-09 376-03 50 mg Capsule shaped L and U on eitherside of breakline (Scored) P22 377-09 377-03 100 mg Capsule shaped LU P23 378-09 378-03 Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Keep container tightly closed. Protect from light.
LOSARTAN POTASSIUM TABLETS USP Rx Only 25 mg NDC 68180-210-06 30 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 50 mg NDC 68180-211-06 30 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 100 mg NDC 68180-212-06 30 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 25 mg NDC 68180-376-06 30 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 50 mg NDC 68180-377-06 30 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 100 mg NDC 68180-378-06 30 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 25 mg NDC 68180-307-02 1000 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 50 mg NDC 68180-308-02 1000 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 100 mg NDC 68180-309-02 1000 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 25 mg NDC 68180-376-09 90 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 25 mg NDC 68180-376-03 1000 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 50 mg NDC 68180-377-09 90 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 50 mg NDC 68180-377-03 1000 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 100 mg NDC 68180-378-09 90 TABLETS LOSARTAN POTASSIUM TABLETS USP Rx Only 100 mg NDC 68180-378-03 1000 TABLETS image image image image image image image image image image image image image image image 25mg-90s 25 mg-90s 25 mg-1000s 25 mg-1000s 50mg-90s 50 mg - 90s 50mg-1000s 50 mg-1000s 100mg-90s 100mg-90s 100mg-1000s 100mg-1000s

source: label

Packages (0)

No package records.

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": "38431fb6-7157-4be5-929a-0c65b7a29c55", "openfda": {"upc": ["0368180212065", "0368180376033", "0368180210061", "0368180378037", "0368180308027", "0368180376095", "0368180211068", "0368180309024", "0368180377030"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["e5886220-43b7-46e1-9034-5242ba245bd1"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "Losartan Potassium", "product_id": "68180-211_38431fb6-7157-4be5-929a-0c65b7a29c55", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68180-211", "generic_name": "Losartan Potassium", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA078232", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20271231"}