Package 43975-351-03

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 43975-351-03
Digits Only 4397535103
Product NDC 43975-351
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43975-351-03)

Marketing

Marketing Status
Marketed Since 2019-11-27
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": "338098af-3cc9-1639-e063-6394a90a6550", "openfda": {"nui": ["N0000175430"], "upc": ["0343975352034", "0343975350030", "0343975349034", "0343975351037"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["bbbaa057-f587-4eb9-a0d2-463dbcd57661"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43975-351-03)", "package_ndc": "43975-351-03", "marketing_start_date": "20191127"}], "brand_name": "PALIPERIDONE", "product_id": "43975-351_338098af-3cc9-1639-e063-6394a90a6550", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43975-351", "generic_name": "PALIPERIDONE", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PALIPERIDONE", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "6 mg/1"}], "application_number": "ANDA204452", "marketing_category": "ANDA", "marketing_start_date": "20191127", "listing_expiration_date": "20261231"}