allergy relief
Generic: loratadine
Labeler: aaa pharmaceutical, inc.Drug Facts
Product Profile
Brand Name
allergy relief
Generic Name
loratadine
Labeler
aaa pharmaceutical, inc.
Dosage Form
TABLET
Routes
Active Ingredients
loratadine 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
57344-193
Product ID
57344-193_dd2d1af9-217a-07ae-e053-2995a90a7202
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA210722
Listing Expiration
2026-12-31
Marketing Start
2020-08-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57344193
Hyphenated Format
57344-193
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA210722 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (57344-193-17)
- 1 BOTTLE, PLASTIC in 1 CARTON (57344-193-19) / 30 TABLET in 1 BOTTLE, PLASTIC
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dd2d1af9-217a-07ae-e053-2995a90a7202", "openfda": {"upc": ["0099581911867"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["9c8535e3-6a60-4640-b37e-a2260936d9af"], "manufacturer_name": ["AAA PHARMACEUTICAL, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (57344-193-17)", "package_ndc": "57344-193-17", "marketing_start_date": "20200814"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-193-19) / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "57344-193-19", "marketing_start_date": "20220429"}], "brand_name": "Allergy Relief", "product_id": "57344-193_dd2d1af9-217a-07ae-e053-2995a90a7202", "dosage_form": "TABLET", "product_ndc": "57344-193", "generic_name": "Loratadine", "labeler_name": "AAA PHARMACEUTICAL, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA210722", "marketing_category": "ANDA", "marketing_start_date": "20200814", "listing_expiration_date": "20261231"}