Package 51655-507-52

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-507-52
Digits Only 5165550752
Product NDC 51655-507
Product ID 51655-507_490f8fd3-7543-fb69-e063-6294a90a8b21
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (51655-507-52)

Marketing

Marketing Status
Marketed Since 2021-01-13
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": "490f8fd3-7543-fb69-e063-6294a90a8b21", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["dae3314f-3128-787f-e053-2995a90aff19"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (51655-507-52)", "package_ndc": "51655-507-52", "marketing_start_date": "20210113"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "51655-507_490f8fd3-7543-fb69-e063-6294a90a8b21", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51655-507", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA075520", "marketing_category": "ANDA", "marketing_start_date": "20210113", "listing_expiration_date": "20271231"}