Package 67046-1500-3

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1500-3
Digits Only 6704615003
Product NDC 67046-1500
Description

30 CAPSULE in 1 BLISTER PACK (67046-1500-3)

Marketing

Marketing Status
Marketed Since 2025-01-28
Brand nortriptyline hydrochloride
Generic nortriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ccb449d-506d-2098-e063-6394a90a74c8", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045"], "spl_set_id": ["2ccb3fd0-53c9-6015-e063-6294a90a3fd6"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (67046-1500-3)", "package_ndc": "67046-1500-3", "marketing_start_date": "20250128"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "67046-1500_2ccb449d-506d-2098-e063-6394a90a74c8", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "67046-1500", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20250128", "listing_expiration_date": "20261231"}