Package 70518-3933-0

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 70518-3933-0
Digits Only 7051839330
Product NDC 70518-3933
Product ID 70518-3933_347acd42-2ed7-5ebe-e063-6294a90aa34c
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3933-0)

Marketing

Marketing Status
Marketed Since 2023-12-04
Brand quetiapine fumarate
Generic quetiapine fumarate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "347acd42-2ed7-5ebe-e063-6294a90aa34c", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["616483"], "spl_set_id": ["b90390d8-6ebc-48b3-8b4d-6a3ff7d19ef6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3933-0)", "package_ndc": "70518-3933-0", "marketing_start_date": "20231204"}], "brand_name": "Quetiapine Fumarate", "product_id": "70518-3933_347acd42-2ed7-5ebe-e063-6294a90aa34c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-3933", "generic_name": "Quetiapine Fumarate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "400 mg/1"}], "application_number": "ANDA091388", "marketing_category": "ANDA", "marketing_start_date": "20231204", "listing_expiration_date": "20261231"}