Package 49483-732-65

Brand: loratadine 10 mg

Generic: loratadine tablets usp, 10 mg
NDC Package

Package Facts

Identity

Package NDC 49483-732-65
Digits Only 4948373265
Product NDC 49483-732
Description

365 TABLET in 1 BOTTLE (49483-732-65)

Marketing

Marketing Status
Marketed Since 2025-01-25
Brand loratadine 10 mg
Generic loratadine tablets usp, 10 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c80ea14-8491-4d26-e063-6294a90aecf0", "openfda": {"upc": ["0349483732658"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["2c80ea14-8490-4d26-e063-6294a90aecf0"], "manufacturer_name": ["TIME CAP LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 BOTTLE (49483-732-65)", "package_ndc": "49483-732-65", "marketing_start_date": "20250125"}], "brand_name": "Loratadine 10 mg", "product_id": "49483-732_2c80ea14-8491-4d26-e063-6294a90aecf0", "dosage_form": "TABLET", "product_ndc": "49483-732", "generic_name": "Loratadine Tablets USP, 10 mg", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine 10 mg", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA219223", "marketing_category": "ANDA", "marketing_start_date": "20250125", "listing_expiration_date": "20261231"}