Package 16714-836-01

Brand: ziprasidone

Generic: ziprasidone
NDC Package

Package Facts

Identity

Package NDC 16714-836-01
Digits Only 1671483601
Product NDC 16714-836
Product ID 16714-836_cbe5f617-d390-54a0-2849-585abd37300f
Description

60 CAPSULE in 1 BOTTLE (16714-836-01)

Marketing

Marketing Status
Marketed Since 2018-07-26
Brand ziprasidone
Generic ziprasidone
Sample Package No

Linked Drug Pages (1)

ziprasidone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cbe5f617-d390-54a0-2849-585abd37300f", "openfda": {"upc": ["0316714836010", "0316714835013"], "unii": ["216X081ORU"], "rxcui": ["313776", "313777", "313778", "314286"], "spl_set_id": ["0071a228-21cc-56a6-dcc9-a7a6ceea758c"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (16714-836-01)", "package_ndc": "16714-836-01", "marketing_start_date": "20180726"}], "brand_name": "ziprasidone", "product_id": "16714-836_cbe5f617-d390-54a0-2849-585abd37300f", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "16714-836", "generic_name": "ziprasidone", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ziprasidone", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA077565", "marketing_category": "ANDA", "marketing_start_date": "20180726", "listing_expiration_date": "20261231"}