NDC codes

FDA NDC Directory
Product NDC (as listed)61314-624Labeler and product segments. Claims need a package NDC.
Product NDC at billing width61314-0624Add 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 NDC11-digit (billing)PackageCopy
61314-624-9461314062494613140624941 VIAL, SINGLE-DOSE in 1 CARTON (61314-624-94) / .05 mL in 1 VIAL, SINGLE-DOSEMarketed from Dec 12, 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)
Cimerli
Generic name (nonproprietary)
ranibizumab-eqrn
Active ingredients
Ranibizumab — .3 mg/.05mL
Dosage form
Injection, Solution
Route
Intravitreal
Labeler
Sandoz IncNDC labeler code 61314
Product type
Prescription drug
Marketing category
BLA — Biologics License ApplicationApplication BLA 761165
Marketing start
Listing expires
Other FDA classes
Vascular Endothelial Growth Factor Inhibitors (Mechanism)
Identifiers
Product ID 61314-624_0bfab18c-289a-42a1-b426-0fc2274a7a3eSPL ID 0bfab18c-289a-42a1-b426-0fc2274a7a3eSPL set ID 4b383d74-4830-4587-95f7-c32a39268df7RxCUI 2612675, 2612681, 2612684, 2612687UNII ZL1R02VT79
Pharmacologic class
Vascular Endothelial Growth Factor Inhibitor

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 codeMed-Code curated

J2778 — Injection, ranibizumab, 0.1 mg

Billing unit: 0.1 mg. Units on the claim = dose given ÷ 0.1 mg.

Ranibizumab biosimilars and the ranibizumab implant have their own HCPCS codes.

Administration

Intravitreal injection procedure (CPT 67028)

The intravitreal injection is reported as a separate procedure from the drug supplied.

How CPT relates to drug billing

NDC on a medical claim

N461314062494 followed by a unit qualifier and the quantity

Package 61314-0624-94. 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 .

Indications (excerpt from the label)

CIMERLI is indicated for the treatment of patients with: CIMERLI, a vascular endothelial growth factor (VEGF) inhibitor, is indicated for the treatment of patients with: • Neovascular (Wet) Age-Related Macular Degeneration (AMD) ( 1.1 ) • Macular Edema Following Retinal Vein Occlusion (RVO) ( 1.2 ) • Diabetic Macular Edema (DME) ( 1.3 ) • Diabetic Retinopathy (DR) ( 1.4 ) • Myopic Choroidal Neovascularization (mCNV) ( 1.5 ) 1.1 Neovascular (Wet) Age-Related Macular Degeneration (AMD) 1.2 Macular Edema Following Retinal Vein Occlusion (RVO) 1.3 Diabetic Macular Edema (DME) 1.4 Diabetic Retinopathy (DR) 1.5 Myopic Choroidal Neovascularization (mCNV)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61314-624

What is NDC 61314-624?
61314-624 is the product NDC for Cimerli (ranibizumab-eqrn), Ranibizumab .3 mg/.05mL injection, solution, listed with the FDA by Sandoz Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cimerli (Ranibizumab-eqrn).
What is the active ingredient?
Ranibizumab.
Who is the labeler?
Sandoz Inc, NDC labeler code 61314. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cimerli?
3 other product NDCs are listed under this name. See all Cimerli NDCs.
Is there a related HCPCS / J-code?
Yes: J2778, Injection, ranibizumab, 0.1 mg. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Cimerli NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Cimerliranibizumab-eqrnRanibizumab .5 mg/.05mLInjection, SolutionIntravitrealSandoz Inc61314-62561314-0625-94
Cimerliranibizumab-eqrnRanibizumab .3 mg/.05mLInjection, SolutionIntravitrealCoherus BioSciences Inc70114-44070114-0440-01
Cimerliranibizumab-eqrnRanibizumab .5 mg/.05mLInjection, SolutionIntravitrealCoherus BioSciences Inc70114-44170114-0441-01

Other NDCs under BLA 761165

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

FDA NDC Directory listings under BLA 761165
ProductStrengthForm · routeLabelerProduct NDC
Cimerliranibizumab-eqrnRanibizumab .5 mg/.05mLInjection, SolutionIntravitrealSandoz Inc61314-625
Cimerliranibizumab-eqrnRanibizumab .3 mg/.05mLInjection, SolutionIntravitrealCoherus BioSciences Inc70114-440
Cimerliranibizumab-eqrnRanibizumab .5 mg/.05mLInjection, SolutionIntravitrealCoherus BioSciences Inc70114-441

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