What is NDC 24208-539?

24208-539 is the product NDC for Miochol E (acetylcholine chloride) kit, listed with the FDA by Bausch & Lomb Incorporated. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Miochol E (Acetylcholine chloride).

Bausch & Lomb Incorporated, NDC labeler code 24208. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Miochol E?

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.

Miochol E NDC 24208-539 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)24208-539Labeler and product segments. Claims need a package NDC.

Product NDC at billing width24208-0539Add 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
24208-539-20	2420805392024208053920	1 KIT in 1 BLISTER PACK (24208-539-20) * 2 mL in 1 VIAL * 2 mL in 1 AMPULEMarketed from Sep 22, 1993

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): Miochol E
Generic name (nonproprietary): acetylcholine chloride
Dosage form: Kit
Labeler: Bausch & Lomb IncorporatedNDC labeler code 24208
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 020213
Marketing start: Sep 22, 1993
Listing expires: Dec 31, 2027
Identifiers: Product ID 24208-539_19c42ee4-9f98-48da-85ea-52090070c2e2SPL ID 19c42ee4-9f98-48da-85ea-52090070c2e2SPL set ID e701ef07-9499-4b56-931f-f4eb3eedbe24RxCUI 876551, 876553

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N424208053920 followed by a unit qualifier and the quantity

Package 24208-0539-20. 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 Mar 17, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE To obtain miosis of the iris in seconds after delivery of the lens in cataract surgery, in penetrating keratoplasty, iridectomy, and other anterior segment surgery where rapid miosis may be required.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24208-539

What is NDC 24208-539?: 24208-539 is the product NDC for Miochol E (acetylcholine chloride) kit, listed with the FDA by Bausch & Lomb Incorporated. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Miochol E (Acetylcholine chloride).
Who is the labeler?: Bausch & Lomb Incorporated, NDC labeler code 24208. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Miochol E?: 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.

Miochol E (Acetylcholine chloride) NDC 24208-539