Package 25000-608-06

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25000-608-06
Digits Only 2500060806
Product NDC 25000-608
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-608-06)

Marketing

Marketing Status
Marketed Since 2022-05-27
Brand duloxetine
Generic duloxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c8aa863f-eb1f-4b66-9ec6-2af2c7958248", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["3686cde5-f76d-4d16-aa5d-caceb8408f8c"], "manufacturer_name": ["MARKSANS PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-608-06)", "package_ndc": "25000-608-06", "marketing_start_date": "20220527"}], "brand_name": "Duloxetine", "product_id": "25000-608_c8aa863f-eb1f-4b66-9ec6-2af2c7958248", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "25000-608", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "MARKSANS PHARMA LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090723", "marketing_category": "ANDA", "marketing_start_date": "20220527", "listing_expiration_date": "20261231"}