What is NDC 72162-2072?

72162-2072 is the product NDC for Propylthiouracil, Propylthiouracil 50 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Propylthiouracil?

7 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Propylthiouracil NDC 72162-2072 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2072Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2072Add 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
72162-2072-1	72162207201	100 TABLET in 1 BOTTLE (72162-2072-1)Marketed from Aug 15, 2023
72162-2072-2	72162207202	180 TABLET in 1 BOTTLE (72162-2072-2)Marketed from Aug 15, 2023

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): Propylthiouracil
Generic name (nonproprietary): propylthiouracil
Active ingredients: Propylthiouracil — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 080154
Marketing start: Mar 18, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Thyroid Hormone Synthesis Inhibitors (Mechanism)
Identifiers: Product ID 72162-2072_a2a5cff0-be4e-4b04-ad87-7ce9b9f2b0feSPL ID a2a5cff0-be4e-4b04-ad87-7ce9b9f2b0feSPL set ID ae65e8b0-91b2-4a3f-8e1a-279e47eee951RxCUI 198175UNII 721M9407IY
Pharmacologic class: Thyroid Hormone Synthesis Inhibitor

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

N472162207201 followed by a unit qualifier and the quantity

Package 72162-2072-01. 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 Aug 20, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Propylthiouracil is indicated: in patients with Graves’ disease with hyperthyroidism or toxic multinodular goiter who are intolerant of methimazole and for whom surgery or radioactive iodine therapy is not an appropriate treatment option. to ameliorate symptoms of hyperthyroidism in preparation for thyroidectomy or radioactive iodine therapy in patients who are intolerant of methimazole.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2072

What is NDC 72162-2072?: 72162-2072 is the product NDC for Propylthiouracil, Propylthiouracil 50 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Propylthiouracil.
What is the active ingredient?: Propylthiouracil.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Propylthiouracil?: 7 other product NDCs are listed under this name. See all Propylthiouracil 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 Propylthiouracil NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	Teva Pharmaceuticals, Inc.	0480-9242	00480-9242-01
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-314	33342-0314-1133342-0314-1233342-0314-44
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	QUAGEN PHARMACEUTICALS LLC	70752-171	70752-0171-1070752-0171-11
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-2901	71335-2901-01
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	American Health Packaging	68084-964	68084-0964-25
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	Chartwell RX, LLC	62135-606	62135-0606-90
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	Par Health USA, LLC	67253-651	67253-0651-1067253-0651-11

Other NDCs under ANDA 080154

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

FDA NDC Directory listings under ANDA 080154
Product	Strength	Form · route	Labeler	Product NDC
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	QUAGEN PHARMACEUTICALS LLC	70752-171
Propylthiouracil	Propylthiouracil 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-2901