Package 75834-148-30

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 75834-148-30
Digits Only 7583414830
Product NDC 75834-148
Product ID 75834-148_3ca13da1-2f1e-5165-e063-6394a90a17fc
Description

30 TABLET in 1 BOTTLE (75834-148-30)

Marketing

Marketing Status
Marketed Since 2017-12-11
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

fluoxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ca13da1-2f1e-5165-e063-6394a90a17fc", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["f4cbf9a9-1d7f-4aa0-a18d-fba50d49bd2b"], "manufacturer_name": ["NIVAGEN PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (75834-148-30)", "package_ndc": "75834-148-30", "marketing_start_date": "20171211"}], "brand_name": "fluoxetine", "product_id": "75834-148_3ca13da1-2f1e-5165-e063-6394a90a17fc", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "75834-148", "generic_name": "fluoxetine hydrochloride", "labeler_name": "NIVAGEN PHARMACEUTICALS, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA209695", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}