procentra

Generic: dextroamphetamine sulfate

Labeler: independence pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name procentra
Generic Name dextroamphetamine sulfate
Labeler independence pharmaceuticals, llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

dextroamphetamine sulfate 5 mg/5mL

Manufacturer
INDEPENDENCE PHARMACEUTICALS, LLC

Identifiers & Regulatory

Product NDC 21724-701
Product ID 21724-701_06b4c32e-1880-40e9-9de2-0927cb8c1500
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040776
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2014-05-15

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 21724701
Hyphenated Format 21724-701

Supplemental Identifiers

RxCUI
884522 884526
UNII
JJ768O327N

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 procentra (source: ndc)
Generic Name dextroamphetamine sulfate (source: ndc)
Application Number ANDA040776 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (21724-701-05)
source: ndc

Packages (1)

Ingredients (1)

dextroamphetamine sulfate (5 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06b4c32e-1880-40e9-9de2-0927cb8c1500", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884522", "884526"], "spl_set_id": ["1548cce2-fb6b-4f17-8a3b-868933f6c9d6"], "manufacturer_name": ["INDEPENDENCE PHARMACEUTICALS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (21724-701-05)", "package_ndc": "21724-701-05", "marketing_start_date": "20140515"}], "brand_name": "PROCENTRA", "product_id": "21724-701_06b4c32e-1880-40e9-9de2-0927cb8c1500", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "21724-701", "dea_schedule": "CII", "generic_name": "dextroamphetamine sulfate", "labeler_name": "INDEPENDENCE PHARMACEUTICALS, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCENTRA", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "5 mg/5mL"}], "application_number": "ANDA040776", "marketing_category": "ANDA", "marketing_start_date": "20140515", "listing_expiration_date": "20261231"}