NDC codes

FDA NDC Directory
Product NDC (as listed)69918-601Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69918-0601Add 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
69918-601-60699180601606991806016060 POUCH in 1 CARTON (69918-601-60) / 10 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINERMarketed from Feb 26, 2022

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)
Timoptic in Ocudose
Generic name (nonproprietary)
timolol maleate
Active ingredients
Timolol maleate — 5 mg/mL
Dosage form
Solution
Route
Ophthalmic
Labeler
Nordic Pharma, Inc.NDC labeler code 69918
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212592
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 69918-601_7fb75a79-b0ff-4ced-88f5-2509f7c28156SPL ID 7fb75a79-b0ff-4ced-88f5-2509f7c28156SPL set ID 16323b0e-78ae-40e5-be93-04f698dd672bUNII P8Y54F701R
Pharmacologic class
beta-Adrenergic Blocker

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

N469918060160 followed by a unit qualifier and the quantity

Package 69918-0601-60. 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 Preservative-free timolol maleate ophthalmic solution USP in the unit dose vial is indicated in the treatment of elevated intraocular pressure in patients with ocular hypertension or open-angle glaucoma. Preservative-free timolol maleate ophthalmic solution USP in the unit dose vial may be used when a patient is sensitive to the preservative in timolol maleate ophthalmic solution USP, benzalkonium chloride, or when use of a preservative-free topical medication is advisable.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69918-601

What is NDC 69918-601?
69918-601 is the product NDC for Timoptic in Ocudose (timolol maleate), Timolol maleate 5 mg/mL solution, listed with the FDA by Nordic Pharma, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Timoptic in Ocudose (Timolol Maleate).
What is the active ingredient?
Timolol maleate.
Who is the labeler?
Nordic Pharma, Inc., NDC labeler code 69918. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Timoptic in Ocudose?
2 other product NDCs are listed under this name. See all Timoptic in Ocudose 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 Timoptic in Ocudose NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Timoptic in Ocudosetimolol maleateTimolol maleate 3.4 mg/mLSolutionOphthalmicBausch & Lomb Incorporated24208-49824208-0498-34
Timoptic in Ocudosetimolol maleateTimolol maleate 6.8 mg/mLSolutionOphthalmicBausch & Lomb Incorporated24208-49924208-0499-0024208-0499-68

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