Package 43598-632-30

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43598-632-30
Digits Only 4359863230
Product NDC 43598-632
Product ID 43598-632_716e99cb-d17e-d5ca-61aa-3298ab7fee96
Description

30 TABLET, FILM COATED in 1 BOTTLE (43598-632-30)

Marketing

Marketing Status
Marketed Since 2019-01-28
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": "716e99cb-d17e-d5ca-61aa-3298ab7fee96", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["80e52273-9741-6aef-eb24-8a93ead85ba7"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (43598-632-01)", "package_ndc": "43598-632-01", "marketing_start_date": "20190128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43598-632-30)", "package_ndc": "43598-632-30", "marketing_start_date": "20190128"}], "brand_name": "Fluoxetine hydrochloride", "product_id": "43598-632_716e99cb-d17e-d5ca-61aa-3298ab7fee96", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43598-632", "generic_name": "Fluoxetine hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211721", "marketing_category": "ANDA", "marketing_start_date": "20190128", "listing_expiration_date": "20261231"}