Package 77771-114-10

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 77771-114-10
Digits Only 7777111410
Product NDC 77771-114
Description

1000 CAPSULE in 1 BOTTLE (77771-114-10)

Marketing

Marketing Status
Marketed Since 2022-10-24
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1cbec1b3-195b-66c8-e063-6294a90ad5a5", "openfda": {"upc": ["0377771115012", "0377771114015", "0377771114107", "0377771113018", "0377771113100", "0377771115050"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["1a07ebe9-3661-4a48-b8af-9b228875166a"], "manufacturer_name": ["RADHA PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (77771-114-01)", "package_ndc": "77771-114-01", "marketing_start_date": "20221024"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (77771-114-10)", "package_ndc": "77771-114-10", "marketing_start_date": "20221024"}], "brand_name": "Fluoxetine", "product_id": "77771-114_1cbec1b3-195b-66c8-e063-6294a90ad5a5", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "77771-114", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "RADHA 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": "20221024", "listing_expiration_date": "20261231"}