Package 46708-806-30
Brand: paliperidone
Generic: paliperidonePackage Facts
Identity
Package NDC
46708-806-30
Digits Only
4670880630
Product NDC
46708-806
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-806-30)
Marketing
Marketing Status
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": "be30f3cc-55fb-4a74-9778-60573a7f18c6", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["be30f3cc-55fb-4a74-9778-60573a7f18c6"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-806-30)", "package_ndc": "46708-806-30", "marketing_start_date": "20240930"}], "brand_name": "paliperidone", "product_id": "46708-806_be30f3cc-55fb-4a74-9778-60573a7f18c6", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "46708-806", "generic_name": "paliperidone", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "9 mg/1"}], "application_number": "ANDA218330", "marketing_category": "ANDA", "marketing_start_date": "20240930", "listing_expiration_date": "20261231"}