United States · FDA National Drug Code directory

CARISOPRODOL

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
42543-700_51dfd284-b3d8-4b5c-b8d4-b93a070ddb2e
Product NDC
42543-700
Form
TABLET
Composition / generic term
CARISOPRODOL
Labeler
Vensun Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20140731
Source listing expiry
20261231

Source-listed ingredients

  • CARISOPRODOL — 350 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (42543-700-01) · 42543-700-01
  • 500 TABLET in 1 BOTTLE (42543-700-05) · 42543-700-05
  • 1000 TABLET in 1 BOTTLE (42543-700-10) · 42543-700-10

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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