NDC codes

FDA NDC Directory
Product NDC (as listed)16714-099Labeler and product segments. Claims need a package NDC.
Product NDC at billing width16714-0099Add 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
16714-099-011671400990116714009901100 CAPSULE in 1 BOTTLE (16714-099-01)Marketed from Mar 31, 2021

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 — 1 mg/1
Dosage form
Capsule
Route
Oral
Labeler
NORTHSTAR RX LLCNDC labeler code 16714
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206662
Marketing start
Listing expires
Other FDA classes
Calcineurin Inhibitors (Mechanism)
Identifiers
Product ID 16714-099_0e68684e-7947-40a2-b17c-7919e94163a5SPL ID 0e68684e-7947-40a2-b17c-7919e94163a5SPL set ID 875f4962-557e-4e12-ad7b-cb5fb6f2a65fRxCUI 198377, 198378, 313190UNII WM0HAQ4WNMUPC 0316714098012, 0316714099019, 0316714100012
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

N416714009901 followed by a unit qualifier and the quantity

Package 16714-0099-01. 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 are a calcineurin-inhibitor immunosuppressant indicated for the prophylaxis of organ rejection in adult and pediatric patients receiving allogeneic liver, kidney or heart transplants in combination with other immunosuppressants. ( 1.1 ) 1.1 Prophylaxis of Organ Rejection in Kidney, Liver, or Heart Transplant Tacrolimus capsules are 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 )] and heart transplant [see Clinical Studies ( 14.3 )] in combination with other immunosuppressants.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 16714-099

What is NDC 16714-099?
16714-099 is the product NDC for tacrolimus, Tacrolimus 1 mg/1 capsule, listed with the FDA by NORTHSTAR RX LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
tacrolimus.
What is the active ingredient?
Tacrolimus.
Who is the labeler?
NORTHSTAR RX LLC, NDC labeler code 16714. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for tacrolimus?
93 other product NDCs are listed under this name. See all tacrolimus 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 tacrolimus NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
TacrolimusTacrolimus .5 mg/1CapsuleOralAvPAK50268-73650268-0736-15
TacrolimusTacrolimus 1 mg/1CapsuleOralAvPAK50268-73750268-0737-15
TacrolimusTacrolimus .5 mg/1CapsuleOralSafecor Health LLC48433-09248433-0092-20
TacrolimusTacrolimus 1 mg/1CapsuleOralSafecor Health LLC48433-09348433-0093-20
TacrolimusTacrolimus 5 mg/1CapsuleOralSafecor Health LLC48433-09448433-0094-20
TacrolimusTacrolimus .5 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals NY LLC69238-278069238-2780-03
TacrolimusTacrolimus 1 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals NY LLC69238-278169238-2781-03
TacrolimusTacrolimus 5 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals NY LLC69238-278269238-2782-03
TacrolimusTacrolimus 5 mg/mLInjectionIntravenousNexus Pharmaceuticals, LLC14789-13514789-0135-05
TacrolimusTacrolimus .5 mg/1CapsuleOralStellon Biotech Inc.85972-10185972-0101-0185972-0101-30

All 94 tacrolimus NDCs

Other NDCs under ANDA 206662

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

FDA NDC Directory listings under ANDA 206662
ProductStrengthForm · routeLabelerProduct NDC
tacrolimusTacrolimus .5 mg/1CapsuleOralNORTHSTAR RX LLC16714-098
tacrolimusTacrolimus 5 mg/1CapsuleOralNORTHSTAR RX LLC16714-100
tacrolimusTacrolimus 1 mg/1CapsuleOralA-S Medication Solutions50090-5581
tacrolimusTacrolimus .5 mg/1CapsuleOralGlenmark Pharmaceuticals Inc., USA68462-685
tacrolimusTacrolimus 1 mg/1CapsuleOralGlenmark Pharmaceuticals Inc., USA68462-686
tacrolimusTacrolimus 5 mg/1CapsuleOralGlenmark Pharmaceuticals Inc., USA68462-687

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