Package 68788-8568-3

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8568-3
Digits Only 6878885683
Product NDC 68788-8568
Product ID 68788-8568_11725d25-b6d9-4270-856d-418e4353be9f
Description

30 CAPSULE in 1 BOTTLE (68788-8568-3)

Marketing

Marketing Status
Marketed Since 2024-01-18
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": "11725d25-b6d9-4270-856d-418e4353be9f", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["af950b46-07df-4de6-a221-d3d7059b87a1"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-8568-3)", "package_ndc": "68788-8568-3", "marketing_start_date": "20240118"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "68788-8568_11725d25-b6d9-4270-856d-418e4353be9f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68788-8568", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "20240118", "listing_expiration_date": "20261231"}