Package 70518-3752-0

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 70518-3752-0
Digits Only 7051837520
Product NDC 70518-3752
Product ID 70518-3752_3b8ab8c6-edd4-2760-e063-6394a90a11e7
Description

30 CAPSULE in 1 BLISTER PACK (70518-3752-0)

Marketing

Marketing Status
Marketed Since 2023-06-08
Brand fluoxetine
Generic fluoxetine
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": "3b8ab8c6-edd4-2760-e063-6394a90a11e7", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["a1b40d46-5233-49d7-9833-762cb6999012"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3752-0)", "package_ndc": "70518-3752-0", "marketing_start_date": "20230608"}], "brand_name": "Fluoxetine", "product_id": "70518-3752_3b8ab8c6-edd4-2760-e063-6394a90a11e7", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-3752", "generic_name": "Fluoxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076001", "marketing_category": "ANDA", "marketing_start_date": "20230608", "listing_expiration_date": "20261231"}