loratadine
Generic: loratadine
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
loratadine
Generic Name
loratadine
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
loratadine 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5532
Product ID
50090-5532_4e8b7bd8-7ff5-4683-942e-a05187095c81
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA076301
Listing Expiration
2026-12-31
Marketing Start
2005-02-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905532
Hyphenated Format
50090-5532
Supplemental Identifiers
RxCUI
UNII
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 (source: ndc)
Generic Name
loratadine (source: ndc)
Application Number
ANDA076301 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 10 TABLET in 1 BOTTLE (50090-5532-0)
- 30 TABLET in 1 BOTTLE (50090-5532-4)
- 90 TABLET in 1 BOTTLE (50090-5532-5)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4e8b7bd8-7ff5-4683-942e-a05187095c81", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["6f82e0ab-2c01-4afb-8d0f-b0c06819d1b0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-5532-0)", "package_ndc": "50090-5532-0", "marketing_start_date": "20211028"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5532-4)", "package_ndc": "50090-5532-4", "marketing_start_date": "20211028"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5532-5)", "package_ndc": "50090-5532-5", "marketing_start_date": "20210430"}], "brand_name": "Loratadine", "product_id": "50090-5532_4e8b7bd8-7ff5-4683-942e-a05187095c81", "dosage_form": "TABLET", "product_ndc": "50090-5532", "generic_name": "Loratadine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076301", "marketing_category": "ANDA", "marketing_start_date": "20050221", "listing_expiration_date": "20261231"}