Package 72189-505-30

Brand: fluoxetine hcl

Generic: fluoxetine hcl
NDC Package

Package Facts

Identity

Package NDC 72189-505-30
Digits Only 7218950530
Product NDC 72189-505
Description

30 CAPSULE in 1 BOTTLE (72189-505-30)

Marketing

Marketing Status
Marketed Since 2023-08-07
Brand fluoxetine hcl
Generic fluoxetine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4e5941-7088-8be7-e063-6394a90a92e3", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["0259db51-e1ff-6e7a-e063-6394a90abace"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-505-30)", "package_ndc": "72189-505-30", "marketing_start_date": "20230807"}], "brand_name": "Fluoxetine HCL", "product_id": "72189-505_2c4e5941-7088-8be7-e063-6394a90a92e3", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72189-505", "generic_name": "Fluoxetine HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine HCL", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20230807", "listing_expiration_date": "20261231"}