Package 0832-6032-12

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0832-6032-12
Digits Only 0832603212
Product NDC 0832-6032
Product ID 0832-6032_178bf3b7-fdee-454e-9446-822a1077d985
Description

1 BOTTLE in 1 CARTON (0832-6032-12) / 120 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-11-30
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": "178bf3b7-fdee-454e-9446-822a1077d985", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310386"], "spl_set_id": ["be2e4325-feb9-4957-99c0-0a741a2d71a0"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0832-6032-12)  / 120 mL in 1 BOTTLE", "package_ndc": "0832-6032-12", "marketing_start_date": "20221130"}], "brand_name": "Fluoxetine hydrochloride", "product_id": "0832-6032_178bf3b7-fdee-454e-9446-822a1077d985", "dosage_form": "FOR SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0832-6032", "generic_name": "Fluoxetine hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA216953", "marketing_category": "ANDA", "marketing_start_date": "20221115", "listing_expiration_date": "20261231"}