Package 55700-727-30

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 55700-727-30
Digits Only 5570072730
Product NDC 55700-727
Product ID 55700-727_bb8fec7f-1868-42d9-8cfb-a180fe1124e4
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-727-30)

Marketing

Marketing Status
Discontinued 2026-05-31
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": "bb8fec7f-1868-42d9-8cfb-a180fe1124e4", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["4d489d05-e767-498f-8827-c03ebfc512e0"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-727-30)", "package_ndc": "55700-727-30", "marketing_end_date": "20260531", "marketing_start_date": "20190222"}], "brand_name": "Duloxetine", "product_id": "55700-727_bb8fec7f-1868-42d9-8cfb-a180fe1124e4", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "55700-727", "generic_name": "Duloxetine", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20190222"}