NDC codes

FDA NDC Directory
Product NDC (as listed)69238-2088Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69238-2088Add 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
69238-2088-6692382088061 TUBE in 1 CARTON (69238-2088-6) / 60 g in 1 TUBEMarketed from May 4, 2022

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)
Bexarotene
Generic name (nonproprietary)
bexarotene
Active ingredients
Bexarotene — 10 mg/g
Dosage form
Gel
Route
Topical
Labeler
Amneal Pharmaceuticals NY LLCNDC labeler code 69238
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215398
Marketing start
Listing expires
Other FDA classes
Retinoids (Chemical structure)
Identifiers
Product ID 69238-2088_e90bb84a-0b45-4163-92da-d8ed239a0b1dSPL ID e90bb84a-0b45-4163-92da-d8ed239a0b1dSPL set ID 2c21f361-e3d1-45a5-a6e7-df8164e3f90dRxCUI 308724UNII A61RXM4375UPC 0369238208863
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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N469238208806 followed by a unit qualifier and the quantity

Package 69238-2088-06. 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)

INDICATIONS AND USAGE Bexarotene gel, 1% is indicated for the topical treatment of cutaneous lesions in patients with CTCL (Stage IA and IB) who have refractory or persistent disease after other therapies or who have not tolerated other therapies.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69238-2088

What is NDC 69238-2088?
69238-2088 is the product NDC for Bexarotene, Bexarotene 10 mg/g gel, listed with the FDA by Amneal Pharmaceuticals NY LLC. 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?
Amneal Pharmaceuticals NY LLC, NDC labeler code 69238. 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/1CapsuleOralCamber Pharmaceuticals, Inc.31722-38031722-0380-01
BexaroteneBexarotene 75 mg/1CapsuleOralAvKARE42291-07242291-0072-01
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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