NDC codes

FDA NDC Directory
Product NDC (as listed)51525-5901Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51525-5901Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
51525-5901-151525590101100 TABLET in 1 BOTTLE (51525-5901-1)Marketed from Oct 1, 2016

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Carisoprodol
Generic name (nonproprietary)
carisoprodol
Active ingredients
Carisoprodol — 250 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 011792
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 51525-5901_8c92753a-4b60-4ecf-b411-d66665ae493eSPL ID 8c92753a-4b60-4ecf-b411-d66665ae493eSPL set ID 7c9184c0-7a2e-11df-8c8d-0002a5d5c51bRxCUI 730794UNII 21925K482H
Pharmacologic class
Muscle Relaxant

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451525590101 followed by a unit qualifier and the quantity

Package 51525-5901-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Carisoprodol tablets are indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults. Limitation of Use Carisoprodol tablets should only be used for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use has not been established and because acute, painful musculoskeletal conditions are generally of short duration [ see Dosage and Administration (2) ] . Carisoprodol tablets are a muscle relaxant indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults. (1) Limitations of Use • Should only be used for acute treatment periods up to two or three wee…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 011792

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 011792
ProductStrengthForm · routeLabelerProduct NDC
SomacarisoprodolCarisoprodol 350 mg/1TabletOralViatris Specialty LLC0037-2001
SomacarisoprodolCarisoprodol 250 mg/1TabletOralViatris Specialty LLC0037-2250

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