amphetamine sulfate

Generic: amphetamine sulfate tablets

Labeler: dr. reddy's laboratories inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amphetamine sulfate
Generic Name amphetamine sulfate tablets
Labeler dr. reddy's laboratories inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amphetamine sulfate 10 mg/1

Manufacturer
DR. REDDY'S LABORATORIES INC

Identifiers & Regulatory

Product NDC 43598-898
Product ID 43598-898_6804c1a2-f648-b841-1d39-74d8624881e0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212582
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2020-03-01

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 43598898
Hyphenated Format 43598-898

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 sulfate tablets (source: ndc)
Application Number ANDA212582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (43598-898-01)
source: ndc

Packages (1)

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

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": "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"}