Package 68071-3779-3
Brand: duloxetine
Generic: duloxetinePackage Facts
Identity
Package NDC
68071-3779-3
Digits Only
6807137793
Product NDC
68071-3779
Description
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3779-3)
Marketing
Marketing Status
Brand
duloxetine
Generic
duloxetine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d7c292f-ed92-07c0-e063-6294a90ae805", "openfda": {"upc": ["0368071377934"], "unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["2d7c2a64-2ce0-f222-e063-6294a90a9056"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3779-3)", "package_ndc": "68071-3779-3", "marketing_start_date": "20250206"}], "brand_name": "Duloxetine", "product_id": "68071-3779_2d7c292f-ed92-07c0-e063-6294a90ae805", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3779", "generic_name": "Duloxetine", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20261231"}