Package 0555-0953-02

Brand: dextroamphetamine sulfate

Generic: dextroamphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 0555-0953-02
Digits Only 0555095302
Product NDC 0555-0953
Product ID 0555-0953_05934bca-3ed9-4ce3-ba1d-2063930aad63
Description

100 TABLET in 1 BOTTLE (0555-0953-02)

Marketing

Marketing Status
Marketed Since 2001-02-12
Brand dextroamphetamine sulfate
Generic dextroamphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Dextroamphetamine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "05934bca-3ed9-4ce3-ba1d-2063930aad63", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884385", "884386"], "spl_set_id": ["ec2d13f3-d14f-47e4-abe9-7763f95a8e94"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0555-0953-02)", "package_ndc": "0555-0953-02", "marketing_start_date": "20010212"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "0555-0953_05934bca-3ed9-4ce3-ba1d-2063930aad63", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0555-0953", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Sulfate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Sulfate", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA040361", "marketing_category": "ANDA", "marketing_start_date": "20010212", "listing_expiration_date": "20271231"}