What is NDC 72205-178?

72205-178 is the product NDC for pomalidomide, Pomalidomide 3 mg/1 capsule, listed with the FDA by Novadoz Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Novadoz Pharmaceuticals LLC, NDC labeler code 72205. 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 72205-178 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72205-178Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72205-0178Add 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
72205-178-21	7220501782172205017821	21 CAPSULE in 1 BOTTLE, PLASTIC (72205-178-21)Marketed from Sep 2, 2026
72205-178-91	7220501789172205017891	100 CAPSULE in 1 BOTTLE, PLASTIC (72205-178-91)Marketed from Sep 2, 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 — 3 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Novadoz Pharmaceuticals LLCNDC labeler code 72205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210245
Marketing start: Sep 2, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 72205-178_fde61c76-de0c-4b62-98f6-fcc25a559d21SPL ID fde61c76-de0c-4b62-98f6-fcc25a559d21
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

N472205017821 followed by a unit qualifier and the quantity

Package 72205-0178-21. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 72205-178

What is NDC 72205-178?: 72205-178 is the product NDC for pomalidomide, Pomalidomide 3 mg/1 capsule, listed with the FDA by Novadoz Pharmaceuticals LLC. It has 2 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?: Novadoz Pharmaceuticals LLC, NDC labeler code 72205. 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 4 mg/1	CapsuleOral	Novadoz Pharmaceuticals LLC	72205-179	72205-0179-2172205-0179-91
Pomalidomide	Pomalidomide 1 mg/1	CapsuleOral	Sandoz Inc	0781-2354	00781-2354-27
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 210245

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

FDA NDC Directory listings under ANDA 210245
Product	Strength	Form · route	Labeler	Product NDC
pomalidomide	Pomalidomide 2 mg/1	CapsuleOral	Novadoz Pharmaceuticals LLC	72205-177
pomalidomide	Pomalidomide 4 mg/1	CapsuleOral	Novadoz Pharmaceuticals LLC	72205-179