allergy relief 10 mg

Generic: loratadine

Labeler: twin med llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief 10 mg
Generic Name loratadine
Labeler twin med llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
TWIN MED LLC

Identifiers & Regulatory

Product NDC 55681-303
Product ID 55681-303_0e12d44c-f956-c1b1-e063-6394a90a7483
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA210722
Listing Expiration 2026-12-31
Marketing Start 2022-03-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55681303
Hyphenated Format 55681-303

Supplemental Identifiers

RxCUI
311372
UNII
7AJO3BO7QN

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 allergy relief 10 mg (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA210722 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 300 TABLET in 1 BOTTLE (55681-303-03)
source: ndc

Packages (1)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e12d44c-f956-c1b1-e063-6394a90a7483", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["d943f548-aa0d-4476-e053-2a95a90a7bd4"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (55681-303-03)", "package_ndc": "55681-303-03", "marketing_start_date": "20220302"}], "brand_name": "ALLERGY RELIEF 10 mg", "product_id": "55681-303_0e12d44c-f956-c1b1-e063-6394a90a7483", "dosage_form": "TABLET", "product_ndc": "55681-303", "generic_name": "LORATADINE", "labeler_name": "TWIN MED LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALLERGY RELIEF", "brand_name_suffix": "10 mg", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA210722", "marketing_category": "ANDA", "marketing_start_date": "20220302", "listing_expiration_date": "20261231"}