Package 63629-2200-1

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2200-1
Digits Only 6362922001
Product NDC 63629-2200
Product ID 63629-2200_acccc0a2-e2d4-43da-ab03-14c45887df8a
Description

100 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-2200-1)

Marketing

Marketing Status
Marketed Since 2016-08-22
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": "acccc0a2-e2d4-43da-ab03-14c45887df8a", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["248642"], "spl_set_id": ["72e391aa-1a46-4589-8550-f83ac9241cf1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-2200-1)", "package_ndc": "63629-2200-1", "marketing_start_date": "20160822"}], "brand_name": "fluoxetine hydrochloride", "product_id": "63629-2200_acccc0a2-e2d4-43da-ab03-14c45887df8a", "dosage_form": "TABLET, COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63629-2200", "generic_name": "fluoxetine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203836", "marketing_category": "ANDA", "marketing_start_date": "20160822", "listing_expiration_date": "20261231"}