Package 60760-311-90

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-311-90
Digits Only 6076031190
Product NDC 60760-311
Product ID 60760-311_a9de93c3-0169-2836-e053-2995a90aa38d
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (60760-311-90)

Marketing

Marketing Status
Marketed Since 2020-06-30
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": "a9de93c3-0169-2836-e053-2995a90aa38d", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["a9de93d4-2edc-2838-e053-2995a90a8ed6"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (60760-311-90)", "package_ndc": "60760-311-90", "marketing_start_date": "20200630"}], "brand_name": "Fluoxetine", "product_id": "60760-311_a9de93c3-0169-2836-e053-2995a90aa38d", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-311", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20200630", "listing_expiration_date": "20261231"}