Package 46708-741-30

Brand: acitretin

Generic: acitretin
NDC Package

Package Facts

Identity

Package NDC 46708-741-30
Digits Only 4670874130
Product NDC 46708-741
Description

30 CAPSULE in 1 BOTTLE (46708-741-30)

Marketing

Marketing Status
Marketed Since 2024-08-08
Brand acitretin
Generic acitretin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "77011f2b-a2e7-4a43-9ff3-29d73f322319", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["LCH760E9T7"], "rxcui": ["199689", "199690", "894859"], "spl_set_id": ["77011f2b-a2e7-4a43-9ff3-29d73f322319"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (46708-741-30)", "package_ndc": "46708-741-30", "marketing_start_date": "20240808"}], "brand_name": "Acitretin", "product_id": "46708-741_77011f2b-a2e7-4a43-9ff3-29d73f322319", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "46708-741", "generic_name": "Acitretin", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acitretin", "active_ingredients": [{"name": "ACITRETIN", "strength": "10 mg/1"}], "application_number": "ANDA217774", "marketing_category": "ANDA", "marketing_start_date": "20240808", "listing_expiration_date": "20261231"}