Timolol maleate NDC 70069-702

NDC codes

FDA NDC Directory

Product NDC (as listed)70069-702Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70069-0702Add 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
70069-702-01	70069070201	1 BOTTLE in 1 CARTON (70069-702-01) / 10 mL in 1 BOTTLEMarketed from Jul 4, 2024

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): Timolol maleate
Generic name (nonproprietary): timolol maleate
Active ingredients: Timolol maleate — 2.5 mg/mL
Dosage form: Solution/ drops
Route: Ophthalmic
Labeler: Somerset Therapeutics, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217764
Marketing start: Jul 4, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 70069-702_e37dc12f-1930-43d0-87a5-ae1eebff29f6SPL ID e37dc12f-1930-43d0-87a5-ae1eebff29f6SPL set ID 5d60db57-ca24-4cab-a90d-8cf06992a34eRxCUI 1923428, 1992303UNII P8Y54F701RUPC 0370069706015, 0370069703014, 0370069708019, 0370069701010, 0370069702017, 0370069707012
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

N470069070201 followed by a unit qualifier and the quantity

Package 70069-0702-01. 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 Jul 4, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Timolol maleate ophthalmic solution is indicated in the treatment of elevated intraocular pressure in patients with ocular hypertension or open-angle glaucoma.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217764

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 217764
Product	Strength	Form · route	Labeler	Product NDC
Timolol maleate	Timolol maleate 2.5 mg/mL	Solution/ dropsOphthalmic	Somerset Therapeutics, LLC	70069-701
Timolol maleate	Timolol maleate 5 mg/mL	Solution/ dropsOphthalmic	Somerset Therapeutics, LLC	70069-708
Timolol maleate	Timolol maleate 2.5 mg/mL	Solution/ dropsOphthalmic	Somerset Therapeutics, LLC	70069-703
Timolol maleate	Timolol maleate 5 mg/mL	Solution/ dropsOphthalmic	Somerset Therapeutics, LLC	70069-706
Timolol maleate	Timolol maleate 5 mg/mL	Solution/ dropsOphthalmic	Somerset Therapeutics, LLC	70069-707