Package 55111-284-48

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55111-284-48
Digits Only 5511128448
Product NDC 55111-284
Product ID 55111-284_69d11d5f-adf1-142a-b4e2-1bace590eba8
Description

1 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2010-03-24
Brand fluoxetine hydrochloride
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluoxetine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "69d11d5f-adf1-142a-b4e2-1bace590eba8", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313995"], "spl_set_id": ["887fc670-db67-4cfe-967b-46b38375dae5"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (55111-284-48)  / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK", "package_ndc": "55111-284-48", "marketing_start_date": "20100324"}], "brand_name": "Fluoxetine hydrochloride", "product_id": "55111-284_69d11d5f-adf1-142a-b4e2-1bace590eba8", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55111-284", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA078572", "marketing_category": "ANDA", "marketing_start_date": "20100324", "listing_expiration_date": "20261231"}