Package 45865-174-30

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45865-174-30
Digits Only 4586517430
Product NDC 45865-174
Description

30 CAPSULE in 1 BOTTLE (45865-174-30)

Marketing

Marketing Status
Marketed Since 2021-09-08
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1302fc08-d5fb-54b4-e063-6394a90a5275", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["1302fc08-d5fa-54b4-e063-6394a90a5275"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (45865-174-30)", "package_ndc": "45865-174-30", "marketing_start_date": "20210908"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (45865-174-60)", "package_ndc": "45865-174-60", "marketing_start_date": "20210415"}], "brand_name": "Fluoxetine", "product_id": "45865-174_1302fc08-d5fb-54b4-e063-6394a90a5275", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "45865-174", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Medsource Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}