Package 0121-4721-40

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-4721-40
Digits Only 0121472140
Product NDC 0121-4721
Product ID 0121-4721_12f427c0-a74a-4af5-ad77-7282d4d70190
Description

4 TRAY in 1 CASE (0121-4721-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05)

Marketing

Marketing Status
Marketed Since 2002-02-01
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": "12f427c0-a74a-4af5-ad77-7282d4d70190", "openfda": {"upc": ["0301210721045"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310386"], "spl_set_id": ["180a07fd-1f6a-4617-b8e0-f938c65ba273"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TRAY in 1 CASE (0121-4721-40)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05)", "package_ndc": "0121-4721-40", "marketing_start_date": "20020201"}], "brand_name": "Fluoxetine", "product_id": "0121-4721_12f427c0-a74a-4af5-ad77-7282d4d70190", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0121-4721", "generic_name": "FLUOXETINE HYDROCHLORIDE", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA076015", "marketing_category": "ANDA", "marketing_start_date": "20020201", "listing_expiration_date": "20261231"}