Package 68071-4606-3

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 68071-4606-3
Digits Only 6807146063
Product NDC 68071-4606
Product ID 68071-4606_1ab615b2-0f7d-911f-e063-6294a90a1479
Description

30 CAPSULE in 1 BOTTLE (68071-4606-3)

Marketing

Marketing Status
Marketed Since 2018-10-19
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": "1ab615b2-0f7d-911f-e063-6294a90a1479", "openfda": {"upc": ["0368071460636"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["78994632-74b3-951c-e053-2a91aa0ac1c8"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-4606-3)", "package_ndc": "68071-4606-3", "marketing_start_date": "20181019"}], "brand_name": "Fluoxetine", "product_id": "68071-4606_1ab615b2-0f7d-911f-e063-6294a90a1479", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-4606", "generic_name": "Fluoxetine", "labeler_name": "NuCare Pharmaceuticals,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": "20020129", "listing_expiration_date": "20261231"}