soma

Generic: carisoprodol

Labeler: viatris specialty llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name soma
Generic Name carisoprodol
Labeler viatris specialty llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

carisoprodol 250 mg/1

Manufacturer
Viatris Specialty LLC

Identifiers & Regulatory

Product NDC 0037-2250
Product ID 0037-2250_7272db18-d8cf-4bd0-ab9d-37e191a06f18
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA011792
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2007-09-08

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 00372250
Hyphenated Format 0037-2250

Supplemental Identifiers

RxCUI
197446 213695 730794 730918
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 soma (source: ndc)
Generic Name carisoprodol (source: ndc)
Application Number NDA011792 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0037-2250-10)
  • 30 TABLET in 1 BOTTLE, PLASTIC (0037-2250-30)
source: ndc

Packages (2)

Ingredients (1)

carisoprodol (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7272db18-d8cf-4bd0-ab9d-37e191a06f18", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["21925K482H"], "rxcui": ["197446", "213695", "730794", "730918"], "spl_set_id": ["6297cf20-830a-11dc-94c8-0002a5d5c51b"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0037-2250-10)", "package_ndc": "0037-2250-10", "marketing_start_date": "20070908"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (0037-2250-30)", "package_ndc": "0037-2250-30", "marketing_start_date": "20070908"}], "brand_name": "Soma", "product_id": "0037-2250_7272db18-d8cf-4bd0-ab9d-37e191a06f18", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0037-2250", "dea_schedule": "CIV", "generic_name": "Carisoprodol", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Soma", "active_ingredients": [{"name": "CARISOPRODOL", "strength": "250 mg/1"}], "application_number": "NDA011792", "marketing_category": "NDA", "marketing_start_date": "20070908", "listing_expiration_date": "20261231"}