Package 60760-831-00

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 60760-831-00
Digits Only 6076083100
Product NDC 60760-831
Description

100 TABLET in 1 BOTTLE, PLASTIC (60760-831-00)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand loratadine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45750216-7bf6-d3c9-e063-6294a90a16cb", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["2bc586e4-5297-44cf-e063-6294a90a531d"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (60760-831-00)", "package_ndc": "60760-831-00", "marketing_start_date": "20240101"}], "brand_name": "Loratadine", "product_id": "60760-831_45750216-7bf6-d3c9-e063-6294a90a16cb", "dosage_form": "TABLET", "product_ndc": "60760-831", "generic_name": "Loratadine", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA210722", "marketing_category": "ANDA", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}