Package 68180-997-06

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-997-06
Digits Only 6818099706
Product NDC 68180-997
Product ID 68180-997_e905b16a-58b6-4211-9931-dd2047db998a
Description

30 TABLET in 1 BOTTLE (68180-997-06)

Marketing

Marketing Status
Marketed Since 2019-04-09
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": "e905b16a-58b6-4211-9931-dd2047db998a", "openfda": {"upc": ["0368180997061"], "unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["f274f102-67ec-46e7-b248-533be2e3003b"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68180-997-06)", "package_ndc": "68180-997-06", "marketing_start_date": "20190409"}], "brand_name": "Fluoxetine Hydrochloride", "product_id": "68180-997_e905b16a-58b6-4211-9931-dd2047db998a", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68180-997", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine Hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211632", "marketing_category": "ANDA", "marketing_start_date": "20190409", "listing_expiration_date": "20261231"}