Package 16714-867-01

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 16714-867-01
Digits Only 1671486701
Product NDC 16714-867
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-867-01)

Marketing

Marketing Status
Marketed Since 2018-10-15
Brand paliperidone
Generic paliperidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49debc9e-6219-4ebc-8412-ccda62f3a6a2", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["5589ec69-c49c-44a7-9561-bbffeb918d1f"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-867-01)", "package_ndc": "16714-867-01", "marketing_start_date": "20181015"}], "brand_name": "Paliperidone", "product_id": "16714-867_49debc9e-6219-4ebc-8412-ccda62f3a6a2", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "16714-867", "generic_name": "Paliperidone", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "3 mg/1"}], "application_number": "ANDA205618", "marketing_category": "ANDA", "marketing_start_date": "20181015", "listing_expiration_date": "20261231"}