Package 83008-046-30

Brand: Duloxetine

Generic: Duloxetine
NDC Package

Package Facts

Identity

Package NDC 83008-046-30
Digits Only 8300804630
Product NDC 83008-046
Product ID 83008-046_b207672b-4423-4e03-8223-51d62aa7920f
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (83008-046-30)

Marketing

Marketing Status
Discontinued 2026-02-28
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": "b207672b-4423-4e03-8223-51d62aa7920f", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["2163f0f2-95f1-4e2c-9ad3-eaab00f6dbf9"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (83008-046-30)", "package_ndc": "83008-046-30", "marketing_end_date": "20260228", "marketing_start_date": "20240215"}], "brand_name": "Duloxetine", "product_id": "83008-046_b207672b-4423-4e03-8223-51d62aa7920f", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "83008-046", "generic_name": "Duloxetine", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20240215"}