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 61919-878
Product ID 61919-878_47e15e5f-bc13-84ec-e063-6394a90a4bf0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203374
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2019-07-26

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 61919878
Hyphenated Format 61919-878

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 ANDA203374 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 350 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (61919-878-60)
  • 120 TABLET in 1 BOTTLE (61919-878-72)
source: ndc

Packages (2)

61919-878-60 60 TABLET in 1 BOTTLE (61919-878-60) 61919-878-72 120 TABLET in 1 BOTTLE (61919-878-72)

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": "47e15e5f-bc13-84ec-e063-6394a90a4bf0", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["21925K482H"], "rxcui": ["197446"], "spl_set_id": ["8e9bb49a-8cc3-4390-e053-2a95a90a4e0e"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-878-60)", "package_ndc": "61919-878-60", "marketing_start_date": "20190726"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (61919-878-72)", "package_ndc": "61919-878-72", "marketing_start_date": "20190726"}], "brand_name": "Carisoprodol", "product_id": "61919-878_47e15e5f-bc13-84ec-e063-6394a90a4bf0", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "61919-878", "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": "ANDA203374", "marketing_category": "ANDA", "marketing_start_date": "20190726", "listing_expiration_date": "20271231"}