Package 70518-4086-0

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4086-0
Digits Only 7051840860
Product NDC 70518-4086
Product ID 70518-4086_3fa3ddf9-13ce-acd5-e063-6394a90a47fe
Description

30 CAPSULE in 1 BLISTER PACK (70518-4086-0)

Marketing

Marketing Status
Marketed Since 2024-05-25
Brand nortriptyline hydrochloride
Generic nortriptyline hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3fa3ddf9-13ce-acd5-e063-6394a90a47fe", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["27e96d6c-b311-45d2-b879-65c6a4efcfba"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4086-0)", "package_ndc": "70518-4086-0", "marketing_start_date": "20240525"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "70518-4086_3fa3ddf9-13ce-acd5-e063-6394a90a47fe", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4086", "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": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20240525", "listing_expiration_date": "20261231"}