Package 51655-981-26

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-981-26
Digits Only 5165598126
Product NDC 51655-981
Product ID 51655-981_4974d225-9324-04ef-e063-6394a90aa77c
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (51655-981-26)

Marketing

Marketing Status
Marketed Since 2022-04-20
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": "4974d225-9324-04ef-e063-6394a90aa77c", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["dfae4357-b6f9-9a30-e053-2995a90a2667"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (51655-981-26)", "package_ndc": "51655-981-26", "marketing_start_date": "20220420"}], "brand_name": "Fluoxetine", "product_id": "51655-981_4974d225-9324-04ef-e063-6394a90aa77c", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-981", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Northwind Health Company, 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": "20220420", "listing_expiration_date": "20271231"}