Prescription drug · ANDA
Cyclopentolate Hydrochloride NDC 24208-735
Cyclopentolate hydrochloride 10 mg/mL · Solution/ drops · Ophthalmic · Bausch & Lomb Incorporated
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 24208-735-01 | 2420807350124208073501 | 1 BOTTLE, DROPPER in 1 CARTON (24208-735-01) / 2 mL in 1 BOTTLE, DROPPERMarketed from Apr 29, 1994 | |
| 24208-735-06 | 2420807350624208073506 | 1 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
N424208073501followed by a unit qualifier and the quantityPackage 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.
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.
Related NDCs: other Cyclopentolate Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Cyclopentolate Hydrochloride | Cyclopentolate hydrochloride 10 mg/mL | SolutionOphthalmic | Sandoz Inc. | 61314-396 | 61314-0396-0161314-0396-0261314-0396-03 |