Package 43063-878-30

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-878-30
Digits Only 4306387830
Product NDC 43063-878
Product ID 43063-878_32d37947-fcd6-03fe-e063-6394a90a8ec3
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-878-30)

Marketing

Marketing Status
Marketed Since 2018-08-06
Brand duloxetine
Generic duloxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Duloxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32d37947-fcd6-03fe-e063-6394a90a8ec3", "openfda": {"upc": ["0343063878903"], "unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["471fec2a-ce5c-4f1a-954c-edf22999686c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-878-30)", "package_ndc": "43063-878-30", "marketing_start_date": "20180806"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-878-90)", "package_ndc": "43063-878-90", "marketing_start_date": "20200727"}], "brand_name": "Duloxetine", "product_id": "43063-878_32d37947-fcd6-03fe-e063-6394a90a8ec3", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43063-878", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090778", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}