NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2525Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2525Add 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
72162-2525-072162252500721622525001000 TABLET in 1 BOTTLE (72162-2525-0)Marketed from Jul 22, 2025
72162-2525-17216225250172162252501100 TABLET in 1 BOTTLE (72162-2525-1)Marketed from Jul 22, 2025
72162-2525-27216225250272162252502100 TABLET in 1 BOTTLE (72162-2525-2)Marketed from Jul 22, 2025

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 Tablets, USP, 350 mg
Generic name (nonproprietary)
carisoprodol
Active ingredients
Carisoprodol — 350 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211789
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 72162-2525_ad5c9fff-69c8-40a5-97a0-6a51d35fb9d5SPL ID ad5c9fff-69c8-40a5-97a0-6a51d35fb9d5SPL set ID 409b04af-b9fd-4ba5-afa0-3e43466f8d2dRxCUI 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

N472162252500 followed by a unit qualifier and the quantity

Package 72162-2525-00. 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, USP are indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults. Limitation of Use Carisoprodol Tablets, USP 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 Tablet is a muscle relaxant indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults. (1) Limitation of Use : Should only be used for acute treatment periods up to two or thr…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2525

What is NDC 72162-2525?
72162-2525 is the product NDC for Carisoprodol Tablets, USP, 350 mg, Carisoprodol 350 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Carisoprodol Tablets, USP, 350 mg (Carisoprodol).
What is the active ingredient?
Carisoprodol.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Carisoprodol Tablets, USP, 350 mg?
3 other product NDCs are listed under this name. See all Carisoprodol Tablets, USP, 350 mg NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Carisoprodol Tablets, USP, 350 mg NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Carisoprodol Tablets, USP, 350 mgcarisoprodolCarisoprodol 350 mg/1TabletOralGranulation Technology, Inc.63561-012763561-0127-0163561-0127-02
Carisoprodol Tablets, USP, 350 mgcarisoprodolCarisoprodol 350 mg/1TabletOralBryant Ranch Prepack71335-301871335-3018-01
Carisoprodol Tablets, USP, 350 mgcarisoprodolCarisoprodol 350 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-47772789-0477-0172789-0477-3072789-0477-90+2 more

Other NDCs under ANDA 211789

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

FDA NDC Directory listings under ANDA 211789
ProductStrengthForm · routeLabelerProduct NDC
Carisoprodol Tablets, USP, 350 mgcarisoprodolCarisoprodol 350 mg/1TabletOralGranulation Technology, Inc.63561-0127
Carisoprodol Tablets, USP, 350 mgcarisoprodolCarisoprodol 350 mg/1TabletOralBryant Ranch Prepack71335-3018
Carisoprodol Tablets, USP, 350 mgcarisoprodolCarisoprodol 350 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-477

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