NDC codes

FDA NDC Directory
Product NDC (as listed)59746-798Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59746-0798Add 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
59746-798-0159746079801100 CAPSULE, GELATIN COATED in 1 BOTTLE (59746-798-01)Marketed from Nov 30, 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)
Tacrolimus
Generic name (nonproprietary)
tacrolimus
Active ingredients
Tacrolimus.5 mg/1
Dosage form
Capsule, Gelatin coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090802
Marketing start
Listing expires
Other FDA classes
Calcineurin Inhibitors (Mechanism)
Identifiers
Product ID 59746-798_e39f4aa6-bc0f-413d-b855-3bf869c2e2eeSPL ID e39f4aa6-bc0f-413d-b855-3bf869c2e2eeSPL set ID 651bd506-96b0-43e5-a4dd-db03bf9154c9RxCUI 198377, 198378, 313190UNII WM0HAQ4WNM
Pharmacologic class
Calcineurin 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

N459746079801 followed by a unit qualifier and the quantity

Package 59746-0798-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Tacrolimus Capsules USP is a calcineurin-inhibitor immunosuppressant indicated for the prophylaxis of organ rejection in adult and pediatric patients receiving allogeneic liver, kidney, heart, or lung transplants, in combination with other immunosuppressants. ( 1.1 ) 1.1 Prophylaxis of Organ Rejection in Kidney, Liver, Heart, or Lung Transplant Tacrolimus Capsules USP is indicated for the prophylaxis of organ rejection, in adult and pediatric patients receiving allogeneic kidney transplant [see Clinical Studies (14.1) ] , liver transplant [see Clinical Studies (14.2) ] , heart transplant [see Clinical Studies (14.3) ] , or lung transplant [see Clinical Studies (14.4) ] in combination with ot

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 090802

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

FDA NDC Directory listings under ANDA 090802
ProductStrengthForm · routeLabelerProduct NDC
TacrolimusTacrolimus 1 mg/1Capsule, Gelatin coatedOralPanacea Biotec Limited43817-422
TacrolimusTacrolimus .5 mg/1Capsule, Gelatin coatedOralPanacea Biotec Limited43817-421
TacrolimusTacrolimus 5 mg/1Capsule, Gelatin coatedOralPanacea Biotec Limited43817-423
TacrolimusTacrolimus 1 mg/1Capsule, Gelatin coatedOralJubilant Cadista Pharmaceuticals Inc.59746-799
TacrolimusTacrolimus 5 mg/1Capsule, Gelatin coatedOralJubilant Cadista Pharmaceuticals Inc.59746-800

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