Package 51655-100-52

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-100-52
Digits Only 5165510052
Product NDC 51655-100
Description

30 CAPSULE in 1 BOTTLE, DISPENSING (51655-100-52)

Marketing

Marketing Status
Marketed Since 2014-05-20
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": "46e3219e-b656-3d59-e063-6394a90aa00a", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["cb66a702-7670-4a73-98fb-0e63151a1ffb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (51655-100-26)", "package_ndc": "51655-100-26", "marketing_start_date": "20220830"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, DISPENSING (51655-100-52)", "package_ndc": "51655-100-52", "marketing_start_date": "20140520"}], "brand_name": "Fluoxetine", "product_id": "51655-100_46e3219e-b656-3d59-e063-6394a90aa00a", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-100", "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": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20140520", "listing_expiration_date": "20271231"}