carisoprodol

Generic: carisoprodol

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

carisoprodol 350 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-182
Product ID 72789-182_2d689c5f-8cf4-8ea3-e063-6394a90a45bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040188
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-01-20

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 72789182
Hyphenated Format 72789-182

Supplemental Identifiers

RxCUI
197446
UPC
0372789182018
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 ANDA040188 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 350 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-182-01)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-182-90)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (72789-182-95)
  • 120 TABLET in 1 BOTTLE, PLASTIC (72789-182-98)
source: ndc

Packages (4)

72789-182-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-182-01) 72789-182-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-182-90) 72789-182-95 1000 TABLET in 1 BOTTLE, PLASTIC (72789-182-95) 72789-182-98 120 TABLET in 1 BOTTLE, PLASTIC (72789-182-98)

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": "2d689c5f-8cf4-8ea3-e063-6394a90a45bd", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789182018"], "unii": ["21925K482H"], "rxcui": ["197446"], "spl_set_id": ["4626a7a7-c433-4dab-8deb-e6e45de493a6"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-182-01)", "package_ndc": "72789-182-01", "marketing_start_date": "20210426"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-182-90)", "package_ndc": "72789-182-90", "marketing_start_date": "20240502"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72789-182-95)", "package_ndc": "72789-182-95", "marketing_start_date": "20210426"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (72789-182-98)", "package_ndc": "72789-182-98", "marketing_start_date": "20240502"}], "brand_name": "Carisoprodol", "product_id": "72789-182_2d689c5f-8cf4-8ea3-e063-6394a90a45bd", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-182", "dea_schedule": "CIV", "generic_name": "Carisoprodol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carisoprodol", "active_ingredients": [{"name": "CARISOPRODOL", "strength": "350 mg/1"}], "application_number": "ANDA040188", "marketing_category": "ANDA", "marketing_start_date": "20200120", "listing_expiration_date": "20261231"}