allergy relief

Generic: loratadine

Labeler: chain drug marketing association, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name loratadine
Labeler chain drug marketing association, inc.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION, INC.

Identifiers & Regulatory

Product NDC 83324-103
Product ID 83324-103_1f7f07c0-c2f3-34ee-e063-6394a90a4dee
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206214
Listing Expiration 2026-12-31
Marketing Start 2024-08-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324103
Hyphenated Format 83324-103

Supplemental Identifiers

RxCUI
828269
UPC
0635515996892
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 (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA206214 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (83324-103-10) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
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": "1f7f07c0-c2f3-34ee-e063-6394a90a4dee", "openfda": {"upc": ["0635515996892"], "unii": ["7AJO3BO7QN"], "rxcui": ["828269"], "spl_set_id": ["e0cb8057-4755-482d-84f4-9275f7b85cd0"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (83324-103-10)  / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "83324-103-10", "marketing_start_date": "20240812"}], "brand_name": "Allergy Relief", "product_id": "83324-103_1f7f07c0-c2f3-34ee-e063-6394a90a4dee", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "83324-103", "generic_name": "Loratadine", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA206214", "marketing_category": "ANDA", "marketing_start_date": "20240812", "listing_expiration_date": "20261231"}