Package 70518-4017-0

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4017-0
Digits Only 7051840170
Product NDC 70518-4017
Product ID 70518-4017_3f906a91-9a16-c7d6-e063-6394a90ab4d2
Description

30 CAPSULE in 1 BLISTER PACK (70518-4017-0)

Marketing

Marketing Status
Marketed Since 2024-02-09
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": "3f906a91-9a16-c7d6-e063-6394a90ab4d2", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045"], "spl_set_id": ["dd1f4d6f-14cc-44c0-b9d3-bb3d17b557fa"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4017-0)", "package_ndc": "70518-4017-0", "marketing_start_date": "20240209"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "70518-4017_3f906a91-9a16-c7d6-e063-6394a90ab4d2", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4017", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "20240209", "listing_expiration_date": "20261231"}