NDC codes

FDA NDC Directory
Product NDC (as listed)70720-100Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70720-0100Add 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
70720-100-1070720010010707200100101 VIAL, GLASS in 1 CARTON (70720-100-10) / 1 mL in 1 VIAL, GLASS (70720-100-01)Marketed from Apr 2, 2020
70720-100-25707200100257072001002525 VIAL, GLASS in 1 CARTON (70720-100-25) / 1 mL in 1 VIAL, GLASS (70720-100-01)Marketed from Nov 13, 2019

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)
Quzyttir
Generic name (nonproprietary)
cetirizine hydrochloride
Active ingredients
Cetirizine hydrochloride — 10 mg/mL
Dosage form
Injection
Route
Intravenous
Labeler
TerSera Therapeutics LLCNDC labeler code 70720
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 211415
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 70720-100_32f69271-f228-41a9-8133-61cb47d73045SPL ID 32f69271-f228-41a9-8133-61cb47d73045SPL set ID f33e859d-ebc9-4d4f-a57d-204c48760d20RxCUI 2261746, 2261754UNII 64O047KTOAUPC 0370720100107, 0370720100251
Pharmacologic class
Histamine-1 Receptor Antagonist

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N470720010010 followed by a unit qualifier and the quantity

Package 70720-0100-10. 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)

QUZYTTIR ® is indicated for the treatment of acute urticaria in adults and children 6 months of age and older. QUZYTTIR ® is a histamine-1 (H 1 ) receptor antagonist indicated for the treatment of acute urticaria in adults and children 6 months of age and older ( 1 ) Limitations of Use : Not recommended in pediatric patients less than 6 years of age with impaired renal or hepatic function ( 1 ) Limitations of use: QUZYTTIR ® is not recommended in pediatric patients less than 6 years of age with impaired renal or hepatic function.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70720-100

What is NDC 70720-100?
70720-100 is the product NDC for Quzyttir (cetirizine hydrochloride), Cetirizine hydrochloride 10 mg/mL injection, listed with the FDA by TerSera Therapeutics LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Quzyttir (Cetirizine Hydrochloride).
What is the active ingredient?
Cetirizine hydrochloride.
Who is the labeler?
TerSera Therapeutics LLC, NDC labeler code 70720. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Quzyttir?
1 other product NDC are listed under this name. See all Quzyttir 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 Quzyttir NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Quzyttircetirizine hydrochlorideCetirizine hydrochloride 10 mg/mLInjectionIntravenousESTEVE PHARMACEUTICALS, S.A.68118-20068118-0200-1068118-0200-25

Other NDCs under NDA 211415

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

FDA NDC Directory listings under NDA 211415
ProductStrengthForm · routeLabelerProduct NDC
Quzyttircetirizine hydrochlorideCetirizine hydrochloride 10 mg/mLInjectionIntravenousESTEVE PHARMACEUTICALS, S.A.68118-200

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