What is NDC 72988-0035?

72988-0035 is the product NDC for Albothyl (policresulen solution), Policresulen 720 mg/g liquid, listed with the FDA by Lydia Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Albothyl (Policresulen Solution).

Lydia Co., Ltd., NDC labeler code 72988. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Albothyl?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Albothyl NDC 72988-0035 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72988-0035Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72988-0035Add 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
72988-0035-1	72988003501	5 g in 1 BOTTLE (72988-0035-1)Marketed from Jan 23, 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): Albothyl
Generic name (nonproprietary): policresulen solution
Active ingredients: Policresulen — 720 mg/g
Dosage form: Liquid
Route: Oral
Labeler: Lydia Co., Ltd.NDC labeler code 72988
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jan 23, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 72988-0035_001d54ef-148b-e55a-e063-6294a90a7c40SPL ID 001d54ef-148b-e55a-e063-6294a90a7c40SPL set ID f2ea4e1b-a3d7-d063-e053-2a95a90a6d0bUNII 6I19M5GB0G

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

N472988003501 followed by a unit qualifier and the quantity

Package 72988-0035-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 72988-0035

What is NDC 72988-0035?: 72988-0035 is the product NDC for Albothyl (policresulen solution), Policresulen 720 mg/g liquid, listed with the FDA by Lydia Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Albothyl (Policresulen Solution).
What is the active ingredient?: Policresulen.
Who is the labeler?: Lydia Co., Ltd., NDC labeler code 72988. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Albothyl?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Albothyl (Policresulen solution) NDC 72988-0035