Package 70518-4281-0

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4281-0
Digits Only 7051842810
Product NDC 70518-4281
Product ID 70518-4281_4019e178-822a-7317-e063-6394a90a7422
Description

30 CAPSULE in 1 BLISTER PACK (70518-4281-0)

Marketing

Marketing Status
Marketed Since 2025-02-08
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": "4019e178-822a-7317-e063-6394a90a7422", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198047"], "spl_set_id": ["4852a754-2fc1-4c10-a414-dc8a1dfd66a2"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4281-0)", "package_ndc": "70518-4281-0", "marketing_start_date": "20250208"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "70518-4281_4019e178-822a-7317-e063-6394a90a7422", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4281", "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": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20250208", "listing_expiration_date": "20261231"}