Package 60687-659-01

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-659-01
Digits Only 6068765901
Product NDC 60687-659
Product ID 60687-659_235a6eb9-d960-13f0-e063-6394a90a5e8b
Description

100 BLISTER PACK in 1 CARTON (60687-659-01) / 1 CAPSULE in 1 BLISTER PACK (60687-659-11)

Marketing

Marketing Status
Marketed Since 2022-07-21
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluoxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "235a6eb9-d960-13f0-e063-6394a90a5e8b", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["7bee936b-0130-4a6b-a974-956aef5486d9"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-659-01)  / 1 CAPSULE in 1 BLISTER PACK (60687-659-11)", "package_ndc": "60687-659-01", "marketing_start_date": "20220721"}], "brand_name": "Fluoxetine", "product_id": "60687-659_235a6eb9-d960-13f0-e063-6394a90a5e8b", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60687-659", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20220721", "listing_expiration_date": "20261231"}