amphetamine sulfate

Generic: amphetamine sulfate

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amphetamine sulfate
Generic Name amphetamine sulfate
Labeler lannett company, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amphetamine sulfate 10 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-2525
Product ID 0527-2525_23880d0f-9eea-4ef3-95aa-10fc11fcfa6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212901
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2020-05-25

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 05272525
Hyphenated Format 0527-2525

Supplemental Identifiers

RxCUI
884655 1600695
UPC
0305272524378 0305272525375
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 sulfate (source: ndc)
Application Number ANDA212901 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0527-2525-37)
source: ndc

Packages (1)

0527-2525-37 100 TABLET in 1 BOTTLE (0527-2525-37)

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": "23880d0f-9eea-4ef3-95aa-10fc11fcfa6c", "openfda": {"upc": ["0305272524378", "0305272525375"], "unii": ["6DPV8NK46S"], "rxcui": ["884655", "1600695"], "spl_set_id": ["85a015a7-a1a0-4b04-8bc4-7aacd0c84742"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0527-2525-37)", "package_ndc": "0527-2525-37", "marketing_start_date": "20200601"}], "brand_name": "AMPHETAMINE SULFATE", "product_id": "0527-2525_23880d0f-9eea-4ef3-95aa-10fc11fcfa6c", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0527-2525", "dea_schedule": "CII", "generic_name": "amphetamine sulfate", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPHETAMINE SULFATE", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA212901", "marketing_category": "ANDA", "marketing_start_date": "20200525", "listing_expiration_date": "20261231"}