Package 70518-1835-0

Brand: ziprasidone hydrochloride

Generic: ziprasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1835-0
Digits Only 7051818350
Product NDC 70518-1835
Description

30 CAPSULE in 1 BLISTER PACK (70518-1835-0)

Marketing

Marketing Status
Marketed Since 2019-01-30
Brand ziprasidone hydrochloride
Generic ziprasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b33c442-08d0-369d-e063-6394a90a4cb6", "openfda": {"unii": ["216X081ORU"], "rxcui": ["314286"], "spl_set_id": ["56370be6-42a2-4962-acdc-22b7c6e0e7fe"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1835-0)", "package_ndc": "70518-1835-0", "marketing_start_date": "20190130"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-1835-1)  / 1 CAPSULE in 1 POUCH (70518-1835-2)", "package_ndc": "70518-1835-1", "marketing_start_date": "20191021"}], "brand_name": "ziprasidone hydrochloride", "product_id": "70518-1835_4b33c442-08d0-369d-e063-6394a90a4cb6", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1835", "generic_name": "ziprasidone hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20190130", "listing_expiration_date": "20271231"}