Package 43063-722-30

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-722-30
Digits Only 4306372230
Product NDC 43063-722
Product ID 43063-722_414b1374-fc77-1888-e063-6394a90ad253
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (43063-722-30)

Marketing

Marketing Status
Marketed Since 2016-10-27
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": "414b1374-fc77-1888-e063-6394a90ad253", "openfda": {"upc": ["0343063722305"], "unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["ba4edb34-82ac-4c98-8abd-fd6176838c78"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-722-30)", "package_ndc": "43063-722-30", "marketing_start_date": "20161027"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "43063-722_414b1374-fc77-1888-e063-6394a90ad253", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "43063-722", "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": "20160601", "listing_expiration_date": "20261231"}