carisoprodol tablets, usp, 350 mg
Generic: carisoprodol
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
carisoprodol tablets, usp, 350 mg
Generic Name
carisoprodol
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
carisoprodol 350 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-477
Product ID
72789-477_41d80caa-d146-cdc1-e063-6294a90a8dc3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211789
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2025-05-11
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789477
Hyphenated Format
72789-477
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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 tablets, usp, 350 mg (source: ndc)
Generic Name
carisoprodol (source: ndc)
Application Number
ANDA211789 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 350 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (72789-477-01)
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-477-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (72789-477-90)
- 1000 TABLET in 1 BOTTLE, PLASTIC (72789-477-95)
- 120 TABLET in 1 BOTTLE, PLASTIC (72789-477-98)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41d80caa-d146-cdc1-e063-6294a90a8dc3", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789477909"], "unii": ["21925K482H"], "rxcui": ["197446"], "spl_set_id": ["1f08f4af-37c2-49b5-a4e3-284414f866fa"], "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 (72789-477-01)", "package_ndc": "72789-477-01", "marketing_start_date": "20250511"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-477-30)", "package_ndc": "72789-477-30", "marketing_start_date": "20251023"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-477-90)", "package_ndc": "72789-477-90", "marketing_start_date": "20250806"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72789-477-95)", "package_ndc": "72789-477-95", "marketing_start_date": "20250511"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (72789-477-98)", "package_ndc": "72789-477-98", "marketing_start_date": "20250812"}], "brand_name": "Carisoprodol Tablets, USP, 350 mg", "product_id": "72789-477_41d80caa-d146-cdc1-e063-6294a90a8dc3", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-477", "dea_schedule": "CIV", "generic_name": "Carisoprodol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carisoprodol Tablets, USP, 350 mg", "active_ingredients": [{"name": "CARISOPRODOL", "strength": "350 mg/1"}], "application_number": "ANDA211789", "marketing_category": "ANDA", "marketing_start_date": "20250511", "listing_expiration_date": "20261231"}