NDC codes

FDA NDC Directory
Product NDC (as listed)36800-706Labeler and product segments. Claims need a package NDC.
Product NDC at billing width36800-0706Add 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
36800-706-22368000706223680007062215 BLISTER PACK in 1 CARTON (36800-706-22) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Aug 16, 2023

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

Generic name (nonproprietary)
loratadine, pseudoephedrine sulfate
Active ingredients
Loratadine — 10 mg/1Pseudoephedrine sulfate — 240 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Topco Associates LLCNDC labeler code 36800
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075989
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)
Identifiers
Product ID 36800-706_790d8277-d9af-46bb-ae3a-dfbf49b3d1beSPL ID 790d8277-d9af-46bb-ae3a-dfbf49b3d1beSPL set ID 32945cd9-60d4-4dc0-96e6-9ed28ffce3fbRxCUI 1117562UNII 7AJO3BO7QN, Y9DL7QPE6B
Pharmacologic class
alpha-Adrenergic Agonist

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

N436800070622 followed by a unit qualifier and the quantity

Package 36800-0706-22. 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)

Uses • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • sneezing • itchy, watery eyes • runny nose • itching of the nose or throat • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies • reduces swelling of nasal passages • temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 36800-706

What is NDC 36800-706?
36800-706 is the product NDC for topcare allergy and congestion relief, Loratadine 10 mg/1; Pseudoephedrine sulfate 240 mg/1 tablet, extended release, listed with the FDA by Topco Associates LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
topcare allergy and congestion relief (Loratadine, pseudoephedrine sulfate).
What is the active ingredient?
Loratadine, Pseudoephedrine sulfate.
Who is the labeler?
Topco Associates LLC, NDC labeler code 36800. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for topcare allergy and congestion relief?
1 other product NDC are listed under this name. See all topcare allergy and congestion relief 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 topcare allergy and congestion relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
topcare allergy and congestion reliefloratadine, pseudoephedrine sulfateLoratadine 5 mg/1; Pseudoephedrine sulfate 120 mg/1Tablet, Film coated, Extended releaseOralTopco Associates LLC36800-61136800-0611-65

Other NDCs under ANDA 075989

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

FDA NDC Directory listings under ANDA 075989
ProductStrengthForm · routeLabelerProduct NDC
allergy congestion reliefloratadine, pseudoephedrine sulfateLoratadine 10 mg/1; Pseudoephedrine sulfate 240 mg/1Tablet, Extended releaseOralKroger Company30142-846
allergy dloratadine, pseudoephedrine sulfateLoratadine 10 mg/1; Pseudoephedrine sulfate 240 mg/1Tablet, Extended releaseOralL. Perrigo Company0113-9004
Allergy Relief Dloratadine, pseudoephedrine sulfateLoratadine 10 mg/1; Pseudoephedrine sulfate 240 mg/1Tablet, Extended releaseOralWalgreen Company0363-2010
kirkland signature allerclear d 24 hrloratadine, pseudoephedrine sulfateLoratadine 10 mg/1; Pseudoephedrine sulfate 240 mg/1Tablet, Extended releaseOralCostco Wholesale Company63981-138

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