Package 70518-3920-1

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3920-1
Digits Only 7051839201
Product NDC 70518-3920
Product ID 70518-3920_3ba347e0-d74e-af63-e063-6394a90ae90f
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3920-1)

Marketing

Marketing Status
Marketed Since 2025-06-18
Brand nortriptyline hydrochloride
Generic nortriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Nortriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ba347e0-d74e-af63-e063-6394a90ae90f", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["522d0cd8-d84d-4961-a525-4527fce44c3c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3920-1)", "package_ndc": "70518-3920-1", "marketing_start_date": "20250618"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "70518-3920_3ba347e0-d74e-af63-e063-6394a90ae90f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3920", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "20231121", "listing_expiration_date": "20261231"}