NDC codes

FDA NDC Directory
Product NDC (as listed)63629-2234Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-2234Add 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
63629-2234-163629223401636292234011 BOTTLE in 1 CARTON (63629-2234-1) / 60 CAPSULE in 1 BOTTLEMarketed from Mar 22, 2021

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)
Nitisinone
Generic name (nonproprietary)
nitisinone
Active ingredients
Nitisinone — 2 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 63629
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211041
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C9 Inhibitors (Mechanism)Cytochrome P450 2E1 Inducers (Mechanism)Hydroxyphenylpyruvate Dioxygenase Inhibitors (Mechanism)Organic Anion Transporter 1 Inhibitors (Mechanism)Organic Anion Transporter 3 Inhibitors (Mechanism)
Identifiers
Product ID 63629-2234_a6f7c9c3-8dbd-4e67-bed6-6a1c1ca122dbSPL ID a6f7c9c3-8dbd-4e67-bed6-6a1c1ca122dbSPL set ID b7c38003-6899-4508-a69a-aef1231de22cRxCUI 351173UNII K5BN214699
Pharmacologic class
4-Hydroxyphenyl-Pyruvate Dioxygenase 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 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

N463629223401 followed by a unit qualifier and the quantity

Package 63629-2234-01. 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 .

Indications (excerpt from the label)

Nitisinone capsules are indicated for the treatment of adult and pediatric patients with hereditary tyrosinemia type 1 (HT-1) in combination with dietary restriction of tyrosine and phenylalanine. Nitisinone is a hydroxy-phenylpyruvate dioxygenase inhibitor indicated for the treatment of adult and pediatric patients with hereditary tyrosinemia type 1 (HT-1) in combination with dietary restriction of tyrosine and phenylalanine.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63629-2234

What is NDC 63629-2234?
63629-2234 is the product NDC for Nitisinone, Nitisinone 2 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nitisinone.
What is the active ingredient?
Nitisinone.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 63629. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nitisinone?
13 other product NDCs are listed under this name. See all Nitisinone 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 Nitisinone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NitisinoneNitisinone 2 mg/1CapsuleOralEton Pharmaceuticals, Inc.71863-11971863-0119-60
NitisinoneNitisinone 5 mg/1CapsuleOralEton Pharmaceuticals, Inc.71863-12071863-0120-60
NitisinoneNitisinone 10 mg/1CapsuleOralEton Pharmaceuticals, Inc.71863-12171863-0121-60
NitisinoneNitisinone 20 mg/1CapsuleOralEton Pharmaceuticals, Inc.71863-12271863-0122-60
NitisinoneNitisinone 20 mg/1CapsuleOralAnalog Pharma70505-22070505-0220-60
NitisinoneNitisinone 2 mg/1CapsuleOralAnalog Pharma70505-20270505-0202-60
NitisinoneNitisinone 5 mg/1CapsuleOralAnalog Pharma70505-20570505-0205-60
NitisinoneNitisinone 10 mg/1CapsuleOralAnalog Pharma70505-21070505-0210-60
NitisinoneNitisinone 2 mg/1CapsuleOralPar Health USA, LLC0254-302000254-3020-02
NitisinoneNitisinone 5 mg/1CapsuleOralPar Health USA, LLC0254-302100254-3021-02

All 14 Nitisinone NDCs

Other NDCs under ANDA 211041

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

FDA NDC Directory listings under ANDA 211041
ProductStrengthForm · routeLabelerProduct NDC
NitisinoneNitisinone 2 mg/1CapsuleOralPar Health USA, LLC0254-3020
NitisinoneNitisinone 5 mg/1CapsuleOralPar Health USA, LLC0254-3021
NitisinoneNitisinone 10 mg/1CapsuleOralPar Health USA, LLC0254-3022
NitisinoneNitisinone 10 mg/1CapsuleOralBryant Ranch Prepack63629-2233
NitisinoneNitisinone 5 mg/1CapsuleOralBryant Ranch Prepack63629-2235

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