loratadine and pseudoephedrine sulfate (30142-724)

Drug Facts

Product Profile

Brand Name loratadine and pseudoephedrine sulfate

Generic Name loratadine and pseudoephedrine sulfate

Labeler the kroger company

Dosage Form TABLET, FILM COATED, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

loratadine 10 mg/1, pseudoephedrine sulfate 240 mg/1

Manufacturer

The Kroger Company

Identifiers & Regulatory

Product NDC 30142-724

Product ID 30142-724_33835307-f778-2003-e063-6294a90a9362

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA076557

Listing Expiration 2026-12-31

Marketing Start 2004-11-17

Pharmacologic Class

Classes

adrenergic alpha-agonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 30142724

Hyphenated Format 30142-724

Supplemental Identifiers

RxCUI

1117562

UNII

7AJO3BO7QN Y9DL7QPE6B

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 loratadine and pseudoephedrine sulfate (source: ndc)

Generic Name loratadine and pseudoephedrine sulfate (source: ndc)

Application Number ANDA076557 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

10 mg/1
240 mg/1

source: ndc

Packaging

15 BLISTER PACK in 1 CARTON (30142-724-15) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
10 BLISTER PACK in 1 CARTON (30142-724-69) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (2)

30142-724-15 15 BLISTER PACK in 1 CARTON (30142-724-15) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK 30142-724-69 10 BLISTER PACK in 1 CARTON (30142-724-69) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

loratadine (10 mg/1) pseudoephedrine sulfate (240 mg/1)

Linked Drug Pages (1)

Loratadine and Pseudoephedrine Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "33835307-f778-2003-e063-6294a90a9362", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["43e53450-9630-4161-8008-22267a785343"], "manufacturer_name": ["The Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 BLISTER PACK in 1 CARTON (30142-724-15)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "30142-724-15", "marketing_start_date": "20041117"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (30142-724-69)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "30142-724-69", "marketing_start_date": "20041117"}], "brand_name": "Loratadine and Pseudoephedrine Sulfate", "product_id": "30142-724_33835307-f778-2003-e063-6294a90a9362", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "30142-724", "generic_name": "Loratadine and Pseudoephedrine Sulfate", "labeler_name": "The Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine and Pseudoephedrine Sulfate", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}, {"name": "PSEUDOEPHEDRINE SULFATE", "strength": "240 mg/1"}], "application_number": "ANDA076557", "marketing_category": "ANDA", "marketing_start_date": "20041117", "listing_expiration_date": "20261231"}