NDC codes

FDA NDC Directory
Product NDC (as listed)59762-1205Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59762-1205Add 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
59762-1205-659762120506597621205061 CARTON in 1 KIT (59762-1205-6) / 1 BOTTLE, GLASS in 1 CARTON (59762-1205-4) / 60 mL in 1 BOTTLE, GLASSMarketed from Jul 22, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Sirolimus
Generic name (nonproprietary)
sirolimus
Active ingredients
Sirolimus — 1 mg/mL
Dosage form
Solution
Route
Oral
Labeler
Mylan Pharmaceuticals Inc.NDC labeler code 59762
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 021083
Marketing start
Listing expires
Other FDA classes
Decreased Immunologic Activity (Physiologic effect)Protein Kinase Inhibitors (Mechanism)mTOR Inhibitors (Mechanism)
Identifiers
Product ID 59762-1205_d6830896-6f5a-4c2b-8ddd-f539a4950c4aSPL ID d6830896-6f5a-4c2b-8ddd-f539a4950c4a
Pharmacologic class
Kinase Inhibitor; mTOR Inhibitor Immunosuppressant

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

N459762120506 followed by a unit qualifier and the quantity

Package 59762-1205-06. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 59762-1205

What is NDC 59762-1205?
59762-1205 is the product NDC for Sirolimus, Sirolimus 1 mg/mL solution, listed with the FDA by Mylan Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sirolimus.
What is the active ingredient?
Sirolimus.
Who is the labeler?
Mylan Pharmaceuticals Inc., NDC labeler code 59762. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sirolimus?
36 other product NDCs are listed under this name. See all Sirolimus 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 Sirolimus NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
sirolimusSirolimus .5 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-90260687-0902-21
sirolimusSirolimus .5 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-444970518-4449-00
SirolimusSirolimus 1 mg/mLSolutionOralRising Pharma Holdings, Inc.16571-80616571-0806-06
sirolimusSirolimus .5 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-437670518-4376-00
SirolimusSirolimus 1 mg/mLSolutionOralCamber Pharmaceuticals, Inc.31722-31631722-0316-31
SirolimusSirolimus 1 mg/1TabletOralREMEDYREPACK INC.70518-379570518-3795-00
sirolimusSirolimus 1 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-77265841-0772-0165841-0772-77
sirolimusSirolimus 2 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-77365841-0773-0165841-0773-77
sirolimusSirolimus 1 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-35168382-0351-0168382-0351-77
sirolimusSirolimus 2 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-35268382-0352-0168382-0352-77

All 37 Sirolimus NDCs

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