Package 16714-722-04

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-722-04
Digits Only 1671472204
Product NDC 16714-722
Product ID 16714-722_a7fb6b36-0508-4287-83c0-976f0f767265
Description

1000 CAPSULE in 1 BOTTLE (16714-722-04)

Marketing

Marketing Status
Marketed Since 2008-01-31
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": "a7fb6b36-0508-4287-83c0-976f0f767265", "openfda": {"upc": ["0316714720029"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["97960730-432e-4e94-bb4e-62a3157270a8"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (16714-722-02)", "package_ndc": "16714-722-02", "marketing_start_date": "20080131"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (16714-722-03)", "package_ndc": "16714-722-03", "marketing_start_date": "20080131"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (16714-722-04)", "package_ndc": "16714-722-04", "marketing_start_date": "20080131"}], "brand_name": "Fluoxetine", "product_id": "16714-722_a7fb6b36-0508-4287-83c0-976f0f767265", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16714-722", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20261231"}