Package 72888-157-39

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72888-157-39
Digits Only 7288815739
Product NDC 72888-157
Product ID 72888-157_47ca5d0b-0a49-87d1-e063-6394a90a1edb
Description

473 mL in 1 BOTTLE (72888-157-39)

Marketing

Marketing Status
Marketed Since 2022-06-14
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": "47ca5d0b-0a49-87d1-e063-6394a90a1edb", "openfda": {"upc": ["0372888157399"], "unii": ["00FN6IH15D"], "rxcui": ["312036"], "spl_set_id": ["bef9e24d-e730-4801-ab25-75e7d6bde225"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (72888-157-39)", "package_ndc": "72888-157-39", "marketing_start_date": "20220614"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "72888-157_47ca5d0b-0a49-87d1-e063-6394a90a1edb", "dosage_form": "SOLUTION", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72888-157", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA217731", "marketing_category": "ANDA", "marketing_start_date": "20220614", "listing_expiration_date": "20271231"}