Package 42708-182-30

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-182-30
Digits Only 4270818230
Product NDC 42708-182
Product ID 42708-182_45872a42-3b7c-bddd-e063-6294a90ae0d5
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (42708-182-30)

Marketing

Marketing Status
Marketed Since 2023-05-26
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package Yes

Linked Drug Pages (1)

Fluoxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45872a42-3b7c-bddd-e063-6294a90ae0d5", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["fc754dff-cecb-fc6b-e053-6394a90ab371"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (42708-182-30)", "package_ndc": "42708-182-30", "marketing_start_date": "20230526"}], "brand_name": "Fluoxetine", "product_id": "42708-182_45872a42-3b7c-bddd-e063-6294a90ae0d5", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42708-182", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "QPharma 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": "20080131", "listing_expiration_date": "20261231"}