Package 0121-0678-16

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-0678-16
Digits Only 0121067816
Product NDC 0121-0678
Product ID 0121-0678_49445e55-d381-44c5-9e91-392f530d6dfc
Description

473 mL in 1 BOTTLE (0121-0678-16)

Marketing

Marketing Status
Marketed Since 2000-08-23
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": "49445e55-d381-44c5-9e91-392f530d6dfc", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["312036"], "spl_set_id": ["3fcabf90-357a-4a06-b680-9572dc28bcfe"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0121-0678-16)", "package_ndc": "0121-0678-16", "marketing_start_date": "20000823"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "0121-0678_49445e55-d381-44c5-9e91-392f530d6dfc", "dosage_form": "SOLUTION", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0121-0678", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA075606", "marketing_category": "ANDA", "marketing_start_date": "20000823", "listing_expiration_date": "20271231"}