Package 0555-0171-78

Brand: mefloquine hydrochloride

Generic: mefloquine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0555-0171-78
Digits Only 0555017178
Product NDC 0555-0171
Description

25 BLISTER PACK in 1 CARTON (0555-0171-78) / 1 TABLET in 1 BLISTER PACK (0555-0171-88)

Marketing

Marketing Status
Marketed Since 2004-01-06
Brand mefloquine hydrochloride
Generic mefloquine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b2b45f8-ed63-4b3c-87c5-801996f5b154", "openfda": {"unii": ["5Y9L3636O3"], "rxcui": ["835913"], "spl_set_id": ["09716a24-d7da-42b2-af29-c03a1b6670bd"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 CARTON (0555-0171-78)  / 1 TABLET in 1 BLISTER PACK (0555-0171-88)", "package_ndc": "0555-0171-78", "marketing_start_date": "20040106"}], "brand_name": "Mefloquine Hydrochloride", "product_id": "0555-0171_4b2b45f8-ed63-4b3c-87c5-801996f5b154", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "0555-0171", "generic_name": "Mefloquine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mefloquine Hydrochloride", "active_ingredients": [{"name": "MEFLOQUINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076392", "marketing_category": "ANDA", "marketing_start_date": "20040106", "listing_expiration_date": "20271231"}