Package 82009-102-05

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82009-102-05
Digits Only 8200910205
Product NDC 82009-102
Product ID 82009-102_3efc8675-fd3f-463f-8170-a80b6a6fa499
Description

500 CAPSULE in 1 BOTTLE (82009-102-05)

Marketing

Marketing Status
Marketed Since 2023-09-01
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": "3efc8675-fd3f-463f-8170-a80b6a6fa499", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["4abbd9d9-e9b1-463d-8f39-f3f50d80f58a"], "manufacturer_name": ["QUALLENT PHARMACEUTICALS HEALTH LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (82009-102-05)", "package_ndc": "82009-102-05", "marketing_start_date": "20230901"}], "brand_name": "Fluoxetine", "product_id": "82009-102_3efc8675-fd3f-463f-8170-a80b6a6fa499", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "82009-102", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "QUALLENT PHARMACEUTICALS HEALTH LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20230901", "listing_expiration_date": "20261231"}