What is NDC 23155-512?

23155-512 is the product NDC for nimodipine, Nimodipine 30 mg/1 capsule, liquid filled, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for nimodipine?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

nimodipine NDC 23155-512 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)23155-512Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23155-0512Add 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
23155-512-00	2315505120023155051200	10 BLISTER PACK in 1 CARTON (23155-512-00) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACKMarketed from Nov 7, 2017
23155-512-30	2315505123023155051230	3 BLISTER PACK in 1 CARTON (23155-512-30) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACKMarketed from Nov 7, 2017

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): nimodipine
Generic name (nonproprietary): nimodipine
Active ingredients: Nimodipine — 30 mg/1
Dosage form: Capsule, Liquid filled
Route: Oral
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.NDC labeler code 23155
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077811
Marketing start: Nov 7, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 23155-512_05594f64-8cb4-4cc0-b1b9-93fb5313b197SPL ID 05594f64-8cb4-4cc0-b1b9-93fb5313b197SPL set ID a323ebd8-ef1b-439b-93d1-ba73a5b0127dRxCUI 198037UNII 57WA9QZ5WH
Pharmacologic class: Dihydropyridine Calcium Channel 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

N423155051200 followed by a unit qualifier and the quantity

Package 23155-0512-00. 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 Aug 16, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Nimodipine is indicated for the improvement of neurological outcome by reducing the incidence and severity of ischemic deficits in patients with subarachnoid hemorrhage from ruptured intracranial berry aneurysms regardless of their post-ictus neurological condition (i.e., Hunt and Hess Grades I to V).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-512

What is NDC 23155-512?: 23155-512 is the product NDC for nimodipine, Nimodipine 30 mg/1 capsule, liquid filled, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: nimodipine.
What is the active ingredient?: Nimodipine.
Who is the labeler?: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for nimodipine?: 2 other product NDCs are listed under this name. See all nimodipine 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 nimodipine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Nimodipine	Nimodipine 60 mg/20mL	SolutionOral	Camber Pharmaceuticals, Inc.	31722-039	31722-0039-47
Nimodipine	Nimodipine 30 mg/1	Capsule, Liquid filledOral	BIONPHARMA INC.	69452-209	69452-0209-1369452-0209-20