Package 70518-4067-0

Brand: Nortriptyline Hydrochloride

Generic: Nortriptyline Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4067-0
Digits Only 7051840670
Product NDC 70518-4067
Product ID 70518-4067_3fa2dd80-c864-6411-e063-6294a90ad9f7
Description

30 CAPSULE in 1 BLISTER PACK (70518-4067-0)

Marketing

Marketing Status
Marketed Since 2024-05-05
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": "3fa2dd80-c864-6411-e063-6294a90ad9f7", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198047"], "spl_set_id": ["c0bf77c7-e53a-4529-b1f0-a30feb8b168d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4067-0)", "package_ndc": "70518-4067-0", "marketing_start_date": "20240505"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "70518-4067_3fa2dd80-c864-6411-e063-6294a90ad9f7", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4067", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "20240505", "listing_expiration_date": "20261231"}