What is NDC 0065-0023?

0065-0023 is the product NDC for Miostat (carbachol), Carbachol .1 mg/mL solution, listed with the FDA by Alcon Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Alcon Laboratories, Inc., NDC labeler code 0065. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Miostat?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Miostat NDC 0065-0023 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0065-0023Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00065-0023Add 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	Copy
0065-0023-15	00065002315	12 VIAL, GLASS in 1 CARTON (0065-0023-15) / 1.5 mL in 1 VIAL, GLASSMarketed from Apr 15, 1974

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Miostat
Generic name (nonproprietary): carbachol
Active ingredients: Carbachol — .1 mg/mL
Dosage form: Solution
Route: Ophthalmic
Labeler: Alcon Laboratories, Inc.NDC labeler code 0065
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 016968
Marketing start: Apr 15, 1974
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Agonists (Mechanism)
Identifiers: Product ID 0065-0023_a76a34d0-2e07-408d-a8c8-d00f2715cad7SPL ID a76a34d0-2e07-408d-a8c8-d00f2715cad7SPL set ID f28d7a56-e079-4a8b-ad81-9a97c780de67RxCUI 308966, 991606UNII 8Y164V895Y
Pharmacologic class: Cholinergic Receptor Agonist

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

N400065002315 followed by a unit qualifier and the quantity

Package 00065-0023-15. 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 Feb 10, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Intraocular use for obtaining miosis during surgery. In addition, MIOSTAT* (carbachol intraocular solution, USP) 0.01% reduces the intensity of IOP elevation in the first 24 hours after cataract surgery.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0065-0023

What is NDC 0065-0023?: 0065-0023 is the product NDC for Miostat (carbachol), Carbachol .1 mg/mL solution, listed with the FDA by Alcon Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Miostat (Carbachol).
What is the active ingredient?: Carbachol.
Who is the labeler?: Alcon Laboratories, Inc., NDC labeler code 0065. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Miostat?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Miostat (Carbachol) NDC 0065-0023