Package 72789-425-30

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-425-30
Digits Only 7278942530
Product NDC 72789-425
Product ID 72789-425_4123bbc5-c72a-e70d-e063-6294a90a2fb4
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (72789-425-30)

Marketing

Marketing Status
Marketed Since 2024-08-07
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": "4123bbc5-c72a-e70d-e063-6294a90a2fb4", "openfda": {"upc": ["0372789425306"], "unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["dbb3cc4d-c36d-495d-b9fc-e5513b2f6b93"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-425-30)", "package_ndc": "72789-425-30", "marketing_start_date": "20240807"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "72789-425_4123bbc5-c72a-e70d-e063-6294a90a2fb4", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-425", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, 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": "20231117", "listing_expiration_date": "20261231"}