What is NDC 24208-023?

24208-023 is the product NDC for Methazolamide, Methazolamide 50 mg/1 tablet, listed with the FDA by Bausch & Lomb Incorporated. It has 4 package NDCs, shown above in 10- and 11-digit form.

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 Methazolamide?

19 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Methazolamide NDC 24208-023 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)24208-023Labeler and product segments. Claims need a package NDC.

Product NDC at billing width24208-0023Add 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
24208-023-01	24208002301	1000 TABLET in 1 BOTTLE (24208-023-01)Marketed from Oct 2, 2020
24208-023-10	24208002310	100 TABLET in 1 BOTTLE (24208-023-10)Marketed from Oct 2, 2020
24208-023-50	24208002350	500 TABLET in 1 BOTTLE (24208-023-50)Marketed from Oct 2, 2020
24208-023-90	24208002390	90 TABLET in 1 BOTTLE (24208-023-90)Marketed from Oct 2, 2020

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): Methazolamide
Generic name (nonproprietary): methazolamide
Active ingredients: Methazolamide — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bausch & Lomb IncorporatedNDC labeler code 24208
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207438
Marketing start: Oct 2, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 24208-023_41d745af-7d7b-dc08-e063-6394a90a2fbfSPL ID 41d745af-7d7b-dc08-e063-6394a90a2fbfSPL set ID 0c0ba5c7-c53e-4e29-a7ff-48fddc5a9258RxCUI 197939, 197940UNII W733B0S9SDUPC 0324208022108, 0324208023105

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

N424208002301 followed by a unit qualifier and the quantity

Package 24208-0023-01. 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 Oct 23, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Methazolamide tablets are indicated in the treatment of ocular conditions where lowering intraocular pressure is likely to be of therapeutic benefit, such as chronic open-angle glaucoma, secondary glaucoma, and preoperatively in acute angle-closure glaucoma where lowering the intraocular pressure is desired before surgery.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24208-023

What is NDC 24208-023?: 24208-023 is the product NDC for Methazolamide, Methazolamide 50 mg/1 tablet, listed with the FDA by Bausch & Lomb Incorporated. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Methazolamide.
What is the active ingredient?: Methazolamide.
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 Methazolamide?: 19 other product NDCs are listed under this name. See all Methazolamide 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 Methazolamide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Methazolamide	Methazolamide 25 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-246	27241-0246-01
Methazolamide	Methazolamide 50 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-247	27241-0247-01
Methazolamide	Methazolamide 50 mg/1	TabletOral	Precision Dose, Inc.	68094-808	68094-0808-50
Methazolamide	Methazolamide 25 mg/1	TabletOral	Precision Dose, Inc.	68094-908	68094-0908-50
Methazolamide	Methazolamide 25 mg/1	TabletOral	NorthStar Rx LLC	72603-166	72603-0166-01
Methazolamide	Methazolamide 50 mg/1	TabletOral	NorthStar Rx LLC	72603-167	72603-0167-01
Methazolamide	Methazolamide 25 mg/1	TabletOral	Bausch & Lomb Incorporated	24208-022	24208-0022-0124208-0022-1024208-0022-50+1 more
Methazolamide	Methazolamide 25 mg/1	TabletOral	Micro Labs Limited	42571-239	42571-0239-0542571-0239-1042571-0239-90
Methazolamide	Methazolamide 50 mg/1	TabletOral	Micro Labs Limited	42571-240	42571-0240-0542571-0240-1042571-0240-90
Methazolamide	Methazolamide 25 mg/1	TabletOral	Bryant Ranch Prepack	72162-1754	72162-1754-01

All 20 Methazolamide NDCs

Other NDCs under ANDA 207438

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

FDA NDC Directory listings under ANDA 207438
Product	Strength	Form · route	Labeler	Product NDC
Methazolamide	Methazolamide 25 mg/1	TabletOral	Micro Labs Limited	42571-239
Methazolamide	Methazolamide 50 mg/1	TabletOral	Micro Labs Limited	42571-240
Methazolamide	Methazolamide 25 mg/1	TabletOral	Bausch & Lomb Incorporated	24208-022