Package 70954-600-10

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70954-600-10
Digits Only 7095460010
Product NDC 70954-600
Product ID 70954-600_0f4f464b-d8a7-400c-ab63-f0510ba8b982
Description

120 mL in 1 BOTTLE, PLASTIC (70954-600-10)

Marketing

Marketing Status
Marketed Since 2022-11-09
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": "0f4f464b-d8a7-400c-ab63-f0510ba8b982", "openfda": {"upc": ["0370954600107"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310386"], "spl_set_id": ["1ffe57c3-6f70-4075-aacb-d87a3990fdea"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, PLASTIC (70954-600-10)", "package_ndc": "70954-600-10", "marketing_start_date": "20221109"}], "brand_name": "Fluoxetine Hydrochloride", "product_id": "70954-600_0f4f464b-d8a7-400c-ab63-f0510ba8b982", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70954-600", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine Hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA216448", "marketing_category": "ANDA", "marketing_start_date": "20221109", "listing_expiration_date": "20271231"}