Package 68071-2275-3

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2275-3
Digits Only 6807122753
Product NDC 68071-2275
Product ID 68071-2275_1d77e6db-8604-5308-e063-6394a90a514d
Description

30 CAPSULE in 1 BOTTLE (68071-2275-3)

Marketing

Marketing Status
Marketed Since 2020-10-09
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": "1d77e6db-8604-5308-e063-6394a90a514d", "openfda": {"upc": ["0368071227536"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["b1409772-e719-67f5-e053-2995a90ab5b6"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-2275-3)", "package_ndc": "68071-2275-3", "marketing_start_date": "20201009"}], "brand_name": "Fluoxetine", "product_id": "68071-2275_1d77e6db-8604-5308-e063-6394a90a514d", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-2275", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}