Package 70518-1359-2

Brand: Fluoxetine

Generic: Fluoxetine Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1359-2
Digits Only 7051813592
Product NDC 70518-1359
Product ID 70518-1359_48e928c8-ff32-4ff8-e063-6394a90ae57f
Description

30 CAPSULE in 1 BLISTER PACK (70518-1359-2)

Marketing

Marketing Status
Marketed Since 2020-05-02
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": "48e928c8-ff32-4ff8-e063-6394a90ae57f", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["aa463a85-3c2e-4465-a548-d2cb590e5db9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1359-2)", "package_ndc": "70518-1359-2", "marketing_start_date": "20200502"}], "brand_name": "Fluoxetine", "product_id": "70518-1359_48e928c8-ff32-4ff8-e063-6394a90ae57f", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1359", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20180809", "listing_expiration_date": "20271231"}