Package 63739-005-32
Brand: ziprasidone hydrochloride
Generic: ziprasidone hydrochloridePackage Facts
Identity
Package NDC
63739-005-32
Digits Only
6373900532
Product NDC
63739-005
Description
4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32) / 10 CAPSULE in 1 BLISTER PACK
Marketing
Marketing Status
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": "2b9c7a48-1373-ab1f-e063-6294a90a5e94", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["db621e08-aa2a-43b9-9d6e-33a633c0f648"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32) / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "63739-005-32", "marketing_end_date": "20260331", "marketing_start_date": "20160111"}], "brand_name": "ziprasidone hydrochloride", "product_id": "63739-005_2b9c7a48-1373-ab1f-e063-6294a90a5e94", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63739-005", "generic_name": "ziprasidone hydrochloride", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20120302"}