Package 43598-898-01

Brand: amphetamine sulfate

Generic: amphetamine sulfate tablets
NDC Package

Package Facts

Identity

Package NDC 43598-898-01
Digits Only 4359889801
Product NDC 43598-898
Product ID 43598-898_6804c1a2-f648-b841-1d39-74d8624881e0
Description

100 TABLET in 1 BOTTLE (43598-898-01)

Marketing

Marketing Status
Marketed Since 2020-03-01
Brand amphetamine sulfate
Generic amphetamine sulfate tablets
Sample Package No

Linked Drug Pages (1)

Amphetamine sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6804c1a2-f648-b841-1d39-74d8624881e0", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["79b9db39-7cdc-5607-f0ce-ac2a2cfd59d5"], "manufacturer_name": ["DR. REDDY'S LABORATORIES INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43598-898-01)", "package_ndc": "43598-898-01", "marketing_start_date": "20200301"}], "brand_name": "Amphetamine sulfate", "product_id": "43598-898_6804c1a2-f648-b841-1d39-74d8624881e0", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43598-898", "dea_schedule": "CII", "generic_name": "Amphetamine Sulfate Tablets", "labeler_name": "DR. REDDY'S LABORATORIES INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amphetamine sulfate", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA212582", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}