Package 60760-908-60

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-908-60
Digits Only 6076090860
Product NDC 60760-908
Description

60 CAPSULE in 1 BOTTLE, PLASTIC (60760-908-60)

Marketing

Marketing Status
Marketed Since 2024-08-28
Brand nortriptyline hydrochloride
Generic nortriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4471fe47-2acd-41a4-e063-6294a90a755b", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045"], "spl_set_id": ["21770082-7a99-520d-e063-6394a90ab9cb"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (60760-908-60)", "package_ndc": "60760-908-60", "marketing_start_date": "20240828"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "60760-908_4471fe47-2acd-41a4-e063-6294a90a755b", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-908", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20231117", "listing_expiration_date": "20261231"}