Package 68001-450-06

Brand: ziprasidone hydrochloride

Generic: ziprasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-450-06
Digits Only 6800145006
Product NDC 68001-450
Product ID 68001-450_326cdd3c-c314-ff98-e063-6294a90a2a20
Description

60 CAPSULE in 1 BOTTLE (68001-450-06)

Marketing

Marketing Status
Marketed Since 2020-08-31
Brand ziprasidone hydrochloride
Generic ziprasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Ziprasidone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "326cdd3c-c314-ff98-e063-6294a90a2a20", "openfda": {"upc": ["0368001450065"], "unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["c0eb7b4d-0264-4eed-8756-51bba3af82fb"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68001-450-06)", "package_ndc": "68001-450-06", "marketing_start_date": "20200831"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "68001-450_326cdd3c-c314-ff98-e063-6294a90a2a20", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68001-450", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204117", "marketing_category": "ANDA", "marketing_start_date": "20200831", "listing_expiration_date": "20261231"}