Package 0904-7045-61

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7045-61
Digits Only 0904704561
Product NDC 0904-7045
Product ID 0904-7045_d893474d-4a41-4771-88d3-25ea749deeff
Description

100 BLISTER PACK in 1 CARTON (0904-7045-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-04-30
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": "d893474d-4a41-4771-88d3-25ea749deeff", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["fdc774b5-c8f2-4daf-94cb-7e73548b541a"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7045-61)  / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-7045-61", "marketing_end_date": "20260430", "marketing_start_date": "20131211"}], "brand_name": "Duloxetine", "product_id": "0904-7045_d893474d-4a41-4771-88d3-25ea749deeff", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0904-7045", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "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_end_date": "20260430", "marketing_start_date": "20131211"}