Package 70518-0787-1
Brand: ziprasidone hydrochloride
Generic: ziprasidone hydrochloridePackage Facts
Identity
Package NDC
70518-0787-1
Digits Only
7051807871
Product NDC
70518-0787
Description
30 POUCH in 1 BOX (70518-0787-1) / 1 CAPSULE in 1 POUCH (70518-0787-2)
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": "4b312260-703f-713e-e063-6294a90a17f2", "openfda": {"unii": ["216X081ORU"], "rxcui": ["313776"], "spl_set_id": ["c9f8f635-cf3f-4c42-8bd1-45bbe19bf97e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-0787-1) / 1 CAPSULE in 1 POUCH (70518-0787-2)", "package_ndc": "70518-0787-1", "marketing_start_date": "20210728"}], "brand_name": "Ziprasidone Hydrochloride", "product_id": "70518-0787_4b312260-703f-713e-e063-6294a90a17f2", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0787", "generic_name": "Ziprasidone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ziprasidone Hydrochloride", "active_ingredients": [{"name": "ZIPRASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204375", "marketing_category": "ANDA", "marketing_start_date": "20171013", "listing_expiration_date": "20271231"}