Package 49483-702-01

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49483-702-01
Digits Only 4948370201
Product NDC 49483-702
Product ID 49483-702_22f2136b-5f0f-f6c7-e063-6394a90a907c
Description

100 CAPSULE in 1 BOTTLE (49483-702-01)

Marketing

Marketing Status
Marketed Since 2022-02-12
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": "22f2136b-5f0f-f6c7-e063-6394a90a907c", "openfda": {"upc": ["0349483703030", "0349483703504", "0349483702019", "0349483703016", "0349483701012", "0349483702101"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["d7a4db7f-cdac-2b36-e053-2995a90a8d64"], "manufacturer_name": ["TIME CAP LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49483-702-01)", "package_ndc": "49483-702-01", "marketing_start_date": "20220212"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (49483-702-10)", "package_ndc": "49483-702-10", "marketing_start_date": "20220212"}], "brand_name": "Fluoxetine", "product_id": "49483-702_22f2136b-5f0f-f6c7-e063-6394a90a907c", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "49483-702", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA075465", "marketing_category": "ANDA", "marketing_start_date": "20220212", "listing_expiration_date": "20261231"}