Package 51655-750-26
Brand: fluoxetine
Generic: fluoxetine hydrochloridePackage Facts
Identity
Package NDC
51655-750-26
Digits Only
5165575026
Product NDC
51655-750
Description
90 CAPSULE in 1 BOTTLE, PLASTIC (51655-750-26)
Marketing
Marketing Status
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": "495166d9-9066-617a-e063-6394a90a2836", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["da6b9b19-2ea1-9a39-e053-2995a90ad730"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (51655-750-26)", "package_ndc": "51655-750-26", "marketing_start_date": "20220901"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (51655-750-52)", "package_ndc": "51655-750-52", "marketing_start_date": "20210712"}], "brand_name": "Fluoxetine", "product_id": "51655-750_495166d9-9066-617a-e063-6394a90a2836", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-750", "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": "10 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20210712", "listing_expiration_date": "20271231"}