Package 51862-016-10

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51862-016-10
Digits Only 5186201610
Product NDC 51862-016
Description

1000 CAPSULE in 1 BOTTLE, PLASTIC (51862-016-10)

Marketing

Marketing Status
Marketed Since 2016-06-01
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": "912a2e7c-3615-4dff-b8b8-27eed882ab3f", "openfda": {"upc": ["0351862016013", "0351862017010", "0351862015016"], "unii": ["00FN6IH15D"], "rxcui": ["198045", "198046", "198047", "317136"], "spl_set_id": ["765d726b-fd4b-4ef7-afd7-9e7e9bf8cae6"], "manufacturer_name": ["Mayne Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (51862-016-10)", "package_ndc": "51862-016-10", "marketing_start_date": "20160601"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "51862-016_912a2e7c-3615-4dff-b8b8-27eed882ab3f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51862-016", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Mayne Pharma 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": "20160601", "listing_expiration_date": "20261231"}