carisoprodol

Generic: carisoprodol

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carisoprodol
Generic Name carisoprodol
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

carisoprodol 350 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-386
Product ID 72189-386_2c4cda4e-be1d-b27b-e063-6394a90a8e19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040792
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2022-10-12

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 72189386
Hyphenated Format 72189-386

Supplemental Identifiers

RxCUI
197446
UNII
21925K482H
NUI
N0000175730 N0000175737

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 ANDA040792 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 350 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-386-30)
  • 120 TABLET in 1 BOTTLE (72189-386-72)
  • 90 TABLET in 1 BOTTLE (72189-386-90)
source: ndc

Packages (3)

Ingredients (1)

carisoprodol (350 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4cda4e-be1d-b27b-e063-6394a90a8e19", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["21925K482H"], "rxcui": ["197446"], "spl_set_id": ["ead8294f-fd27-5c3d-e053-2a95a90a64af"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-386-30)", "package_ndc": "72189-386-30", "marketing_start_date": "20221012"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (72189-386-72)", "package_ndc": "72189-386-72", "marketing_start_date": "20221012"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-386-90)", "package_ndc": "72189-386-90", "marketing_start_date": "20221012"}], "brand_name": "Carisoprodol", "product_id": "72189-386_2c4cda4e-be1d-b27b-e063-6394a90a8e19", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72189-386", "dea_schedule": "CIV", "generic_name": "Carisoprodol", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carisoprodol", "active_ingredients": [{"name": "CARISOPRODOL", "strength": "350 mg/1"}], "application_number": "ANDA040792", "marketing_category": "ANDA", "marketing_start_date": "20221012", "listing_expiration_date": "20261231"}