Package 71205-358-60

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 71205-358-60
Digits Only 7120535860
Product NDC 71205-358
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-60)

Marketing

Marketing Status
Marketed Since 2019-11-14
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": "5761ba46-a046-4deb-93b9-87919fbc17d0", "openfda": {"upc": ["0371205358303"], "unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["e36a6919-568a-4d4a-9920-7a7fe4f3441c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-30)", "package_ndc": "71205-358-30", "marketing_start_date": "20191114"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-60)", "package_ndc": "71205-358-60", "marketing_start_date": "20191114"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-90)", "package_ndc": "71205-358-90", "marketing_start_date": "20191114"}], "brand_name": "Duloxetine", "product_id": "71205-358_5761ba46-a046-4deb-93b9-87919fbc17d0", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71205-358", "generic_name": "Duloxetine", "labeler_name": "Proficient Rx LP", "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": "20170316", "listing_expiration_date": "20261231"}