amphetamine sulfate

Generic: amphetamine

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amphetamine sulfate
Generic Name amphetamine
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amphetamine sulfate 10 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-1564
Product ID 69238-1564_940571ac-35e3-426e-8eb0-386a3987c3b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211139
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2018-09-28

Pharmacologic Class

Classes
central nervous system stimulant [epc] central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692381564
Hyphenated Format 69238-1564

Supplemental Identifiers

RxCUI
884655 1600695
UNII
6DPV8NK46S

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name amphetamine sulfate (source: ndc)
Generic Name amphetamine (source: ndc)
Application Number ANDA211139 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69238-1564-1)
source: ndc

Packages (1)

69238-1564-1 100 TABLET in 1 BOTTLE (69238-1564-1)

Ingredients (1)

amphetamine sulfate (10 mg/1)

Linked Drug Pages (1)

Amphetamine Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "940571ac-35e3-426e-8eb0-386a3987c3b9", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["53d40847-e0d3-48ec-81a7-ec5478553565"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-1564-1)", "package_ndc": "69238-1564-1", "marketing_start_date": "20180928"}], "brand_name": "Amphetamine Sulfate", "product_id": "69238-1564_940571ac-35e3-426e-8eb0-386a3987c3b9", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "69238-1564", "dea_schedule": "CII", "generic_name": "Amphetamine", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amphetamine Sulfate", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA211139", "marketing_category": "ANDA", "marketing_start_date": "20180928", "listing_expiration_date": "20261231"}