Package 68071-5276-1

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5276-1
Digits Only 6807152761
Product NDC 68071-5276
Product ID 68071-5276_1d7912d5-2296-f96e-e063-6294a90acf27
Description

100 CAPSULE in 1 BOTTLE (68071-5276-1)

Marketing

Marketing Status
Marketed Since 2020-06-10
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": "1d7912d5-2296-f96e-e063-6294a90acf27", "openfda": {"upc": ["0368071527612"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["a7bea6e9-cf90-a963-e053-2a95a90a1068"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68071-5276-1)", "package_ndc": "68071-5276-1", "marketing_start_date": "20200610"}], "brand_name": "Fluoxetine", "product_id": "68071-5276_1d7912d5-2296-f96e-e063-6294a90acf27", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-5276", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20150316", "listing_expiration_date": "20261231"}