NDC codes

FDA NDC Directory
Product NDC (as listed)31722-773Labeler and product segments. Claims need a package NDC.
Product NDC at billing width31722-0773Add 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
31722-773-013172207730131722077301100 CAPSULE in 1 BOTTLE (31722-773-01)Marketed from Feb 28, 2026
31722-773-21317220773213172207732121 CAPSULE in 1 BOTTLE (31722-773-21)Marketed from Feb 28, 2026
31722-773-3231722077332317220773326 BLISTER PACK in 1 CARTON (31722-773-32) / 10 CAPSULE in 1 BLISTER PACKMarketed from Feb 28, 2026

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)
Pomalidomide
Generic name (nonproprietary)
pomalidomide
Active ingredients
Pomalidomide — 4 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 210236
Marketing start
Listing expires
Identifiers
Product ID 31722-773_4c3e8f7f-ef41-3672-e063-6294a90ac5d6SPL ID 4c3e8f7f-ef41-3672-e063-6294a90ac5d6SPL set ID 52676691-e171-467c-ae55-b5dcc14062a4RxCUI 1369718, 1369726, 1369730, 1369734UNII D2UX06XLB5UPC 0331722770217, 0331722772211, 0331722773218, 0331722771214
Pharmacologic class
Thalidomide Analog

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

N431722077301 followed by a unit qualifier and the quantity

Package 31722-0773-01. 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)

Pomalidomide is a thalidomide analogue indicated for the treatment of adult patients: • in combination with dexamethasone, for patients with multiple myeloma (MM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy ( 1.1 ). 1.1 Multiple Myeloma Pomalidomide capsules, in combination with dexamethasone, is indicated for adult patients with multiple myeloma (MM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy.…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 31722-773

What is NDC 31722-773?
31722-773 is the product NDC for Pomalidomide, Pomalidomide 4 mg/1 capsule, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Pomalidomide.
What is the active ingredient?
Pomalidomide.
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 Pomalidomide?
42 other product NDCs are listed under this name. See all Pomalidomide 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 Pomalidomide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
pomalidomidePomalidomide 2 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-17772205-0177-2172205-0177-91
pomalidomidePomalidomide 3 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-17872205-0178-2172205-0178-91
pomalidomidePomalidomide 4 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-17972205-0179-2172205-0179-91
PomalidomidePomalidomide 1 mg/1CapsuleOralSandoz Inc0781-235400781-2354-27
PomalidomidePomalidomide 2 mg/1CapsuleOralSandoz Inc0781-235800781-2358-27
PomalidomidePomalidomide 3 mg/1CapsuleOralSandoz Inc0781-236600781-2366-27
PomalidomidePomalidomide 4 mg/1CapsuleOralSandoz Inc0781-236900781-2369-27
pomalidomidePomalidomide 4 mg/1CapsuleOralDr. Reddy's Laboratories Inc.43598-51743598-0517-0143598-0517-21
pomalidomidePomalidomide 3 mg/1CapsuleOralDr. Reddy's Laboratories Inc.43598-51843598-0518-0143598-0518-21
pomalidomidePomalidomide 2 mg/1CapsuleOralDr. Reddy's Laboratories Inc.43598-51943598-0519-0143598-0519-21

All 43 Pomalidomide NDCs

Other NDCs under ANDA 210236

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

FDA NDC Directory listings under ANDA 210236
ProductStrengthForm · routeLabelerProduct NDC
PomalidomidePomalidomide 1 mg/1CapsuleOralCamber Pharmaceuticals, Inc.31722-770
PomalidomidePomalidomide 2 mg/1CapsuleOralCamber Pharmaceuticals, Inc.31722-771
PomalidomidePomalidomide 3 mg/1CapsuleOralCamber Pharmaceuticals, Inc.31722-772

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