Package 68180-999-01

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-999-01
Digits Only 6818099901
Product NDC 68180-999
Product ID 68180-999_71041a6b-43e4-415c-a1a6-dbd55a09a0d6
Description

100 TABLET in 1 BOTTLE (68180-999-01)

Marketing

Marketing Status
Marketed Since 2019-08-07
Brand fluoxetine hydrochloride
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluoxetine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "71041a6b-43e4-415c-a1a6-dbd55a09a0d6", "openfda": {"upc": ["0368180998068", "0368180999065"], "unii": ["I9W7N6B1KJ"], "rxcui": ["248642", "313990"], "spl_set_id": ["dd659085-c32d-4d35-9d4b-bafa2a93f1fb"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68180-999-01)", "package_ndc": "68180-999-01", "marketing_start_date": "20190807"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68180-999-06)", "package_ndc": "68180-999-06", "marketing_start_date": "20190807"}], "brand_name": "Fluoxetine Hydrochloride", "product_id": "68180-999_71041a6b-43e4-415c-a1a6-dbd55a09a0d6", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68180-999", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine Hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA211653", "marketing_category": "ANDA", "marketing_start_date": "20190807", "listing_expiration_date": "20261231"}