Package 70518-2630-2

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 70518-2630-2
Digits Only 7051826302
Product NDC 70518-2630
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-2)

Marketing

Marketing Status
Marketed Since 2020-07-28
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": "4a7b6ca6-8965-4925-e063-6294a90a59eb", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["ac903bda-76af-4aba-9c8a-ebf7066e05ee"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-0)", "package_ndc": "70518-2630-0", "marketing_start_date": "20200316"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-2)", "package_ndc": "70518-2630-2", "marketing_start_date": "20200728"}, {"sample": false, "description": "180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-3)", "package_ndc": "70518-2630-3", "marketing_start_date": "20251009"}], "brand_name": "Duloxetine", "product_id": "70518-2630_4a7b6ca6-8965-4925-e063-6294a90a59eb", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2630", "generic_name": "Duloxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20200316", "listing_expiration_date": "20271231"}