Package 68001-368-04

Brand: duloxetine delayed-release

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-368-04
Digits Only 6800136804
Product NDC 68001-368
Product ID 68001-368_115a0854-7a53-c19e-e063-6294a90a53c7
Description

30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68001-368-04)

Marketing

Marketing Status
Marketed Since 2018-05-21
Brand duloxetine delayed-release
Generic duloxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Duloxetine Delayed-Release ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "115a0854-7a53-c19e-e063-6294a90a53c7", "openfda": {"unii": ["9044SC542W"], "rxcui": ["616402"], "spl_set_id": ["a95cc04c-58e9-487f-8992-ef30df03a3cd"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68001-368-04)", "package_ndc": "68001-368-04", "marketing_start_date": "20180521"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "68001-368_115a0854-7a53-c19e-e063-6294a90a53c7", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68001-368", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20180521", "listing_expiration_date": "20261231"}