Package 70518-2134-4

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2134-4
Digits Only 7051821344
Product NDC 70518-2134
Product ID 70518-2134_49d97d78-d273-dac5-e063-6394a90abdc3
Description

100 POUCH in 1 BOX (70518-2134-4) / 1 CAPSULE in 1 POUCH (70518-2134-5)

Marketing

Marketing Status
Marketed Since 2022-08-09
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": "49d97d78-d273-dac5-e063-6394a90abdc3", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["53747336-dc8d-4d28-8832-5e59ccc5b64c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2134-4)  / 1 CAPSULE in 1 POUCH (70518-2134-5)", "package_ndc": "70518-2134-4", "marketing_start_date": "20220809"}], "brand_name": "Fluoxetine", "product_id": "70518-2134_49d97d78-d273-dac5-e063-6394a90abdc3", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2134", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20190606", "listing_expiration_date": "20271231"}