carisoprodol

Generic: carisoprodol

Labeler: sciegen pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carisoprodol
Generic Name carisoprodol
Labeler sciegen pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

carisoprodol 350 mg/1

Manufacturer
ScieGen Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 50228-109
Product ID 50228-109_f1b2306e-24ae-607d-e053-2a95a90aa908
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203374
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2014-01-27

Pharmacologic Class

Established (EPC)
muscle relaxant [epc]
Physiologic Effect
centrally-mediated muscle relaxation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50228109
Hyphenated Format 50228-109

Supplemental Identifiers

RxCUI
197446
UPC
0350228109017 0350228109307
UNII
21925K482H
NUI
N0000175730 N0000175737

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 carisoprodol (source: ndc)
Generic Name carisoprodol (source: ndc)
Application Number ANDA203374 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 350 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50228-109-01)
  • 500 TABLET in 1 BOTTLE (50228-109-05)
  • 1000 TABLET in 1 BOTTLE (50228-109-10)
  • 30 TABLET in 1 BOTTLE (50228-109-30)
source: ndc

Packages (4)

50228-109-01 100 TABLET in 1 BOTTLE (50228-109-01) 50228-109-05 500 TABLET in 1 BOTTLE (50228-109-05) 50228-109-10 1000 TABLET in 1 BOTTLE (50228-109-10) 50228-109-30 30 TABLET in 1 BOTTLE (50228-109-30)

Ingredients (1)

carisoprodol (350 mg/1)

Linked Drug Pages (1)

CARISOPRODOL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f1b2306e-24ae-607d-e053-2a95a90aa908", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0350228109017", "0350228109307"], "unii": ["21925K482H"], "rxcui": ["197446"], "spl_set_id": ["069ea892-21a6-4703-8dd3-bf19c4406479"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50228-109-01)", "package_ndc": "50228-109-01", "marketing_start_date": "20140127"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50228-109-05)", "package_ndc": "50228-109-05", "marketing_start_date": "20140127"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-109-10)", "package_ndc": "50228-109-10", "marketing_start_date": "20140127"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-109-30)", "package_ndc": "50228-109-30", "marketing_start_date": "20140127"}], "brand_name": "CARISOPRODOL", "product_id": "50228-109_f1b2306e-24ae-607d-e053-2a95a90aa908", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50228-109", "dea_schedule": "CIV", "generic_name": "CARISOPRODOL", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARISOPRODOL", "active_ingredients": [{"name": "CARISOPRODOL", "strength": "350 mg/1"}], "application_number": "ANDA203374", "marketing_category": "ANDA", "marketing_start_date": "20140127", "listing_expiration_date": "20261231"}