What is NDC 0781-2354?

0781-2354 is the product NDC for Pomalidomide, Pomalidomide 1 mg/1 capsule, listed with the FDA by Sandoz Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

Sandoz Inc, NDC labeler code 0781. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pomalidomide NDC 0781-2354 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0781-2354Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00781-2354Add 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 NDC	11-digit (billing)	Package	Copy
0781-2354-27	0078123542700781235427	21 CAPSULE in 1 BOTTLE (0781-2354-27)Marketed from Sep 1, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 1 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Sandoz IncNDC labeler code 0781
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 220741
Marketing start: Sep 1, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 0781-2354_4fcd4978-b2d1-4d1a-b239-717cddb8be1fSPL ID 4fcd4978-b2d1-4d1a-b239-717cddb8be1fSPL set ID 4fcd4978-b2d1-4d1a-b239-717cddb8be1fRxCUI 1369718, 1369726, 1369730, 1369734UNII D2UX06XLB5
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

N400781235427 followed by a unit qualifier and the quantity

Package 00781-2354-27. 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 Apr 15, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Pomalidomide capsules are 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 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0781-2354

What is NDC 0781-2354?: 0781-2354 is the product NDC for Pomalidomide, Pomalidomide 1 mg/1 capsule, listed with the FDA by Sandoz Inc. It has 1 package NDC, 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?: Sandoz Inc, NDC labeler code 0781. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
pomalidomide	Pomalidomide 2 mg/1	CapsuleOral	Novadoz Pharmaceuticals LLC	72205-177	72205-0177-2172205-0177-91
pomalidomide	Pomalidomide 3 mg/1	CapsuleOral	Novadoz Pharmaceuticals LLC	72205-178	72205-0178-2172205-0178-91
pomalidomide	Pomalidomide 4 mg/1	CapsuleOral	Novadoz Pharmaceuticals LLC	72205-179	72205-0179-2172205-0179-91
Pomalidomide	Pomalidomide 2 mg/1	CapsuleOral	Sandoz Inc	0781-2358	00781-2358-27
Pomalidomide	Pomalidomide 3 mg/1	CapsuleOral	Sandoz Inc	0781-2366	00781-2366-27
Pomalidomide	Pomalidomide 4 mg/1	CapsuleOral	Sandoz Inc	0781-2369	00781-2369-27
pomalidomide	Pomalidomide 4 mg/1	CapsuleOral	Dr. Reddy's Laboratories Inc.	43598-517	43598-0517-0143598-0517-21
pomalidomide	Pomalidomide 3 mg/1	CapsuleOral	Dr. Reddy's Laboratories Inc.	43598-518	43598-0518-0143598-0518-21
pomalidomide	Pomalidomide 2 mg/1	CapsuleOral	Dr. Reddy's Laboratories Inc.	43598-519	43598-0519-0143598-0519-21
pomalidomide	Pomalidomide 1 mg/1	CapsuleOral	Dr. Reddy's Laboratories Inc.	43598-520	43598-0520-0143598-0520-21

All 43 Pomalidomide NDCs

Other NDCs under ANDA 220741

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

FDA NDC Directory listings under ANDA 220741
Product	Strength	Form · route	Labeler	Product NDC
Pomalidomide	Pomalidomide 2 mg/1	CapsuleOral	Sandoz Inc	0781-2358
Pomalidomide	Pomalidomide 3 mg/1	CapsuleOral	Sandoz Inc	0781-2366
Pomalidomide	Pomalidomide 4 mg/1	CapsuleOral	Sandoz Inc	0781-2369