Package 68001-595-08

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 68001-595-08
Digits Only 6800159508
Product NDC 68001-595
Description

1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-08)

Marketing

Marketing Status
Marketed Since 2023-07-28
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": "3cc7677d-d409-c32e-e063-6294a90a94f4", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934", "616402"], "spl_set_id": ["1409fc2b-7252-472f-b719-e56141b36da2"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-04)", "package_ndc": "68001-595-04", "marketing_start_date": "20240222"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-05)", "package_ndc": "68001-595-05", "marketing_start_date": "20231110"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-08)", "package_ndc": "68001-595-08", "marketing_start_date": "20230728"}], "brand_name": "Duloxetine", "product_id": "68001-595_3cc7677d-d409-c32e-e063-6294a90a94f4", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68001-595", "generic_name": "Duloxetine", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20230728", "listing_expiration_date": "20261231"}