NDC codes

FDA NDC Directory
Product NDC (as listed)24208-735Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24208-0735Add 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 NDC11-digit (billing)PackageCopy
24208-735-0124208073501242080735011 BOTTLE, DROPPER in 1 CARTON (24208-735-01) / 2 mL in 1 BOTTLE, DROPPERMarketed from Apr 29, 1994
24208-735-0624208073506242080735061 BOTTLE, DROPPER in 1 CARTON (24208-735-06) / 15 mL in 1 BOTTLE, DROPPERMarketed from Apr 29, 1994

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)
Cyclopentolate Hydrochloride
Generic name (nonproprietary)
cyclopentolate hydrochloride
Active ingredients
Cyclopentolate hydrochloride — 10 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
Bausch & Lomb IncorporatedNDC labeler code 24208
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040075
Marketing start
Listing expires
Identifiers
Product ID 24208-735_34fff06e-fa45-478a-b136-e019483fa07dSPL ID 34fff06e-fa45-478a-b136-e019483fa07dSPL set ID ad85b220-6003-4a78-b900-5195ceaf0fd5RxCUI 1298066UNII 736I6971TE

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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N424208073501 followed by a unit qualifier and the quantity

Package 24208-0735-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Cyclopentolate hydrochloride ophthalmic solution is used to produce mydriasis and cycloplegia.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24208-735

What is NDC 24208-735?
24208-735 is the product NDC for Cyclopentolate Hydrochloride, Cyclopentolate hydrochloride 10 mg/mL solution/ drops, listed with the FDA by Bausch & Lomb Incorporated. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cyclopentolate Hydrochloride.
What is the active ingredient?
Cyclopentolate hydrochloride.
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 Cyclopentolate Hydrochloride?
1 other product NDC are listed under this name. See all Cyclopentolate Hydrochloride 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 Cyclopentolate Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Cyclopentolate HydrochlorideCyclopentolate hydrochloride 10 mg/mLSolutionOphthalmicSandoz Inc.61314-39661314-0396-0161314-0396-0261314-0396-03

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