Package 71335-0827-4

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0827-4
Digits Only 7133508274
Product NDC 71335-0827
Description

90 CAPSULE in 1 BOTTLE (71335-0827-4)

Marketing

Marketing Status
Marketed Since 2016-06-29
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": "b9d5a8f5-39f1-425d-93fa-8adf95867fdb", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["02283de9-6087-45f7-a9ce-3b082ce860de"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-0827-1)", "package_ndc": "71335-0827-1", "marketing_start_date": "20160629"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-0827-2)", "package_ndc": "71335-0827-2", "marketing_start_date": "20160629"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-0827-3)", "package_ndc": "71335-0827-3", "marketing_start_date": "20160629"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-0827-4)", "package_ndc": "71335-0827-4", "marketing_start_date": "20160629"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE (71335-0827-5)", "package_ndc": "71335-0827-5", "marketing_start_date": "20160629"}, {"sample": false, "description": "180 CAPSULE in 1 BOTTLE (71335-0827-6)", "package_ndc": "71335-0827-6", "marketing_start_date": "20160629"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (71335-0827-7)", "package_ndc": "71335-0827-7", "marketing_start_date": "20160629"}], "brand_name": "Fluoxetine", "product_id": "71335-0827_b9d5a8f5-39f1-425d-93fa-8adf95867fdb", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0827", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}