Package 71335-1445-1

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 71335-1445-1
Digits Only 7133514451
Product NDC 71335-1445
Product ID 71335-1445_4c5b381d-c201-4208-8118-513704333a05
Description

30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-1445-1)

Marketing

Marketing Status
Marketed Since 2013-12-17
Brand duloxetine
Generic duloxetine
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": "4c5b381d-c201-4208-8118-513704333a05", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["ff118c08-2e64-4416-a996-fd9de45d018a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-1445-1)", "package_ndc": "71335-1445-1", "marketing_start_date": "20131217"}], "brand_name": "Duloxetine", "product_id": "71335-1445_4c5b381d-c201-4208-8118-513704333a05", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-1445", "generic_name": "Duloxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20271231"}