amphetamine sulfate

Generic: amphetamine sulfate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amphetamine sulfate
Generic Name amphetamine sulfate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amphetamine sulfate 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1369
Product ID 72162-1369_b7799b14-8dd8-472b-8279-5f6ba27aa313
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211861
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2020-04-02

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 721621369
Hyphenated Format 72162-1369

Supplemental Identifiers

RxCUI
1600695
UNII
6DPV8NK46S

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 ANDA211861 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-1369-1)
source: ndc

Packages (1)

72162-1369-1 100 TABLET in 1 BOTTLE (72162-1369-1)

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": "b7799b14-8dd8-472b-8279-5f6ba27aa313", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["1600695"], "spl_set_id": ["7f16dd18-bf30-41ef-8981-932da5df0951"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1369-1)", "package_ndc": "72162-1369-1", "marketing_start_date": "20240125"}], "brand_name": "AMPHETAMINE SULFATE", "product_id": "72162-1369_b7799b14-8dd8-472b-8279-5f6ba27aa313", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1369", "dea_schedule": "CII", "generic_name": "amphetamine sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPHETAMINE SULFATE", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA211861", "marketing_category": "ANDA", "marketing_start_date": "20200402", "listing_expiration_date": "20261231"}