Package 63187-457-30

Brand: duloxetine hydrochloride

Generic: duloxetin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-457-30
Digits Only 6318745730
Product NDC 63187-457
Product ID 63187-457_6a8c9e37-5317-4fa9-ab2c-495d0d326c5e
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-457-30)

Marketing

Marketing Status
Marketed Since 2019-01-01
Brand duloxetine hydrochloride
Generic duloxetin hydrochloride
Sample Package No

Linked Drug Pages (1)

Duloxetine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6a8c9e37-5317-4fa9-ab2c-495d0d326c5e", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["510ceafd-8254-428c-b2ff-a167f283cda7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-457-30)", "package_ndc": "63187-457-30", "marketing_start_date": "20190101"}], "brand_name": "Duloxetine hydrochloride", "product_id": "63187-457_6a8c9e37-5317-4fa9-ab2c-495d0d326c5e", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63187-457", "generic_name": "Duloxetin hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine hydrochloride", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090774", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}