NDC codes

FDA NDC Directory
Product NDC (as listed)71432-2003Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71432-2003Add 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
71432-2003-1714322003011 BAG in 1 CARTON (71432-2003-1) / 5 BLISTER PACK in 1 BAG / 10 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Jan 25, 2024

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)
tacrolimus
Generic name (nonproprietary)
tacrolimus extended-release capsules
Active ingredients
Tacrolimus — 5 mg/1
Dosage form
Capsule, Coated, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215012
Marketing start
Listing expires
Other FDA classes
Calcineurin Inhibitors (Mechanism)
Identifiers
Product ID 71432-2003_102bdf7c-9d79-0124-e063-6394a90aced9SPL ID 102bdf7c-9d79-0124-e063-6394a90aced9SPL set ID 08cf2861-2483-405d-a872-a88a5c235f9aRxCUI 1431971, 1431980, 1431985UNII 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

N471432200301 followed by a unit qualifier and the quantity

Package 71432-2003-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 215012

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

FDA NDC Directory listings under ANDA 215012
ProductStrengthForm · routeLabelerProduct NDC
TacrolimusTacrolimus 5 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals NY LLC69238-2782
TacrolimusTacrolimus .5 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals NY LLC69238-2780
TacrolimusTacrolimus 1 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals NY LLC69238-2781
tacrolimustacrolimus extended-release capsulesTacrolimus 1 mg/1Capsule, Coated, Extended releaseOralChengdu Suncadia Medicine Co., Ltd.71432-2002
tacrolimustacrolimus extended-release capsulesTacrolimus .5 mg/1Capsule, Coated, Extended releaseOralChengdu Suncadia Medicine Co., Ltd.71432-2001

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