NDC codes

FDA NDC Directory
Product NDC (as listed)31722-380Labeler and product segments. Claims need a package NDC.
Product NDC at billing width31722-0380Add 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
31722-380-01317220380011 BOTTLE in 1 CARTON (31722-380-01) / 100 CAPSULE in 1 BOTTLEMarketed from May 21, 2025

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)
Bexarotene
Generic name (nonproprietary)
bexarotene
Active ingredients
Bexarotene — 75 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Camber Pharmaceuticals, Inc.NDC labeler code 31722
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208628
Marketing start
Listing expires
Other FDA classes
Retinoids (Chemical structure)
Identifiers
Product ID 31722-380_fbea212d-1296-43aa-bae6-9f2b56020b10SPL ID fbea212d-1296-43aa-bae6-9f2b56020b10SPL set ID 374c42b1-3d7f-4ca3-9d3a-2a111286f7caRxCUI 308725UNII A61RXM4375UPC 0331722380010
Pharmacologic class
Retinoid

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

N431722038001 followed by a unit qualifier and the quantity

Package 31722-0380-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Bexarotene capsules are indicated for the treatment of cutaneous manifestations of cutaneous T-cell lymphoma in patients who are refractory to at least one prior systemic therapy. Bexarotene is a retinoid indicated for the treatment of cutaneous manifestations of cutaneous T-cell lymphoma in patients who are refractory to at least one prior systemic therapy. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 31722-380

What is NDC 31722-380?
31722-380 is the product NDC for Bexarotene, Bexarotene 75 mg/1 capsule, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bexarotene.
What is the active ingredient?
Bexarotene.
Who is the labeler?
Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bexarotene?
7 other product NDCs are listed under this name. See all Bexarotene 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 Bexarotene NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BexaroteneBexarotene 75 mg/1CapsuleOralAvKARE42291-07242291-0072-01
BexaroteneBexarotene 10 mg/gGelTopicalAmneal Pharmaceuticals NY LLC69238-208869238-2088-06
bexaroteneBexarotene 75 mg/1Capsule, Liquid filledOralActavis Pharma, Inc.0591-283200591-2832-01
BexaroteneBexarotene 75 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-125069238-1250-01
BexaroteneBexarotene 75 mg/1CapsuleOralUpsher-Smith Laboratories, Inc.0832-028500832-0285-00
BexaroteneBexarotene 75 mg/1Capsule, Liquid filledOralANI Pharmaceuticals, Inc.43975-31543975-0315-10
BexaroteneBexarotene 75 mg/1Capsule, Liquid filledOralMylan Pharmaceuticals Inc.0378-695500378-6955-01

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