NDC codes

FDA NDC Directory
Product NDC (as listed)72189-386Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0386Add 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
72189-386-307218903863030 TABLET in 1 BOTTLE (72189-386-30)Marketed from Oct 12, 2022
72189-386-7272189038672120 TABLET in 1 BOTTLE (72189-386-72)Marketed from Oct 12, 2022
72189-386-907218903869090 TABLET in 1 BOTTLE (72189-386-90)Marketed from Oct 12, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 350 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Direct_Rx
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040792
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 72189-386_2c4cda4e-be1d-b27b-e063-6394a90a8e19SPL ID 2c4cda4e-be1d-b27b-e063-6394a90a8e19SPL set ID ead8294f-fd27-5c3d-e053-2a95a90a64afRxCUI 197446UNII 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

N472189038630 followed by a unit qualifier and the quantity

Package 72189-0386-30. 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)].

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040792

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

FDA NDC Directory listings under ANDA 040792
ProductStrengthForm · routeLabelerProduct NDC
carisoprodolCarisoprodol 350 mg/1TabletOralREMEDYREPACK INC.70518-3792
carisoprodolCarisoprodol 250 mg/1TabletOralAurobindo Pharma Limited65862-693
carisoprodolCarisoprodol 350 mg/1TabletOralBryant Ranch Prepack71335-9613
carisoprodolCarisoprodol 350 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3421
carisoprodolCarisoprodol 250 mg/1TabletOralRising Pharma Holdings, Inc.16571-780
carisoprodolCarisoprodol 350 mg/1TabletOralRising Pharma Holdings, Inc.16571-781
carisoprodolCarisoprodol 250 mg/1TabletOralAsclemed USA, Inc.76420-852
carisoprodolCarisoprodol 350 mg/1TabletOralAsclemed USA, Inc.76420-853
carisoprodolCarisoprodol 350 mg/1TabletOralAurobindo Pharma Limited65862-158

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