What is NDC 10702-014?

10702-014 is the product NDC for Betaxolol Hydrochloride, Betaxolol hydrochloride 20 mg/1 tablet, coated, listed with the FDA by KVK-TECH, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

KVK-TECH, INC., NDC labeler code 10702. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Betaxolol Hydrochloride?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Betaxolol Hydrochloride NDC 10702-014

NDC codes

FDA NDC Directory

Product NDC (as listed)10702-014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10702-0014Add 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
10702-014-01	1070200140110702001401	100 TABLET, COATED in 1 BOTTLE (10702-014-01)Marketed from Nov 2, 2011

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): Betaxolol Hydrochloride
Generic name (nonproprietary): betaxolol hydrochloride
Active ingredients: Betaxolol hydrochloride — 20 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: KVK-TECH, INC.NDC labeler code 10702
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078962
Marketing start: Nov 2, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 10702-014_1757ca78-c783-c977-e063-6294a90a7862SPL ID 1757ca78-c783-c977-e063-6294a90a7862SPL set ID f3b50bbb-df03-4ed7-9d8d-180edc2abd54RxCUI 1297753, 1297757UNII 6X97D2XT0O
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N410702001401 followed by a unit qualifier and the quantity

Package 10702-0014-01. 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 Apr 30, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Betaxolol tablets, USP is indicated in the management of hypertension. It may be used alone or concomitantly with other antihypertensive agents, particularly thiazide-type diuretics.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10702-014

What is NDC 10702-014?: 10702-014 is the product NDC for Betaxolol Hydrochloride, Betaxolol hydrochloride 20 mg/1 tablet, coated, listed with the FDA by KVK-TECH, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Betaxolol Hydrochloride.
What is the active ingredient?: Betaxolol hydrochloride.
Who is the labeler?: KVK-TECH, INC., NDC labeler code 10702. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Betaxolol Hydrochloride?: 2 other product NDCs are listed under this name. See all Betaxolol 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 Betaxolol Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Betaxolol Hydrochloride	Betaxolol hydrochloride 10 mg/1	Tablet, CoatedOral	KVK-TECH, INC.	10702-013	10702-0013-01
Betaxolol Hydrochloride	Betaxolol hydrochloride 5.6 mg/mL	Solution/ dropsOphthalmic	Sandoz Inc	61314-245	61314-0245-0161314-0245-0261314-0245-03

Other NDCs under ANDA 078962

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

FDA NDC Directory listings under ANDA 078962
Product	Strength	Form · route	Labeler	Product NDC
Betaxolol Hydrochloride	Betaxolol hydrochloride 10 mg/1	Tablet, CoatedOral	KVK-TECH, INC.	10702-013