Package 72189-067-30

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-067-30
Digits Only 7218906730
Product NDC 72189-067
Description

30 CAPSULE in 1 BOTTLE (72189-067-30)

Marketing

Marketing Status
Marketed Since 2020-01-07
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": "2be78ca4-349b-418a-e063-6294a90a0b01", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["9b8d8da5-8c06-0942-e053-2995a90aa2c9"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-067-30)", "package_ndc": "72189-067-30", "marketing_start_date": "20200107"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-067-90)", "package_ndc": "72189-067-90", "marketing_start_date": "20200107"}], "brand_name": "FLUOXETINE", "product_id": "72189-067_2be78ca4-349b-418a-e063-6294a90a0b01", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72189-067", "generic_name": "FLUOXETINE HYDROCHLORIDE", "labeler_name": "DIRECT RX", "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": "20200107", "listing_expiration_date": "20261231"}