Package 82804-139-30

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-139-30
Digits Only 8280413930
Product NDC 82804-139
Product ID 82804-139_661ec73c-d893-446a-83c3-218b06889962
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (82804-139-30)

Marketing

Marketing Status
Marketed Since 2024-09-06
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": "661ec73c-d893-446a-83c3-218b06889962", "openfda": {"upc": ["0382804139309"], "unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["661ec73c-d893-446a-83c3-218b06889962"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (82804-139-30)", "package_ndc": "82804-139-30", "marketing_start_date": "20240906"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "82804-139_661ec73c-d893-446a-83c3-218b06889962", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82804-139", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Proficient Rx LP", "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": "20231117", "listing_expiration_date": "20261231"}