NDC codes

FDA NDC Directory
Product NDC (as listed)51672-2108Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51672-2108Add 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
51672-2108-1516722108011 BOTTLE in 1 CARTON (51672-2108-1) / 240 mL in 1 BOTTLEMarketed from Dec 8, 2016
51672-2108-8516722108081 BOTTLE in 1 CARTON (51672-2108-8) / 120 mL in 1 BOTTLEMarketed from Dec 8, 2016

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)
Childrens Loratadine Sugar FreeSuffix: Sugar Free
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 5 mg/5mL
Dosage form
Solution
Route
Oral
Labeler
Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 201865
Marketing start
Listing expires
Identifiers
Product ID 51672-2108_5698ca72-fe88-2bd1-e063-6394a90aee88SPL ID 5698ca72-fe88-2bd1-e063-6394a90aee88SPL set ID 96a76906-58ad-40cd-be27-4ea254e298c5RxCUI 692783UNII 7AJO3BO7QN

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

N451672210801 followed by a unit qualifier and the quantity

Package 51672-2108-01. 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)

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-2108

What is NDC 51672-2108?
51672-2108 is the product NDC for Childrens Loratadine Sugar Free (loratadine), Loratadine 5 mg/5mL solution, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Childrens Loratadine Sugar Free (Loratadine).
What is the active ingredient?
Loratadine.
Who is the labeler?
Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Childrens Loratadine Sugar Free?
6 other product NDCs are listed under this name. See all Childrens Loratadine Sugar Free 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 Childrens Loratadine Sugar Free NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Childrens Loratadine Sugar FreeloratadineLoratadine 5 mg/5mLSolutionOralSTRATEGIC SOURCING SERVICES LLC70677-105870677-1058-01
Childrens Loratadine Sugar FreeloratadineLoratadine 5 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-828668788-8286-01
Childrens Loratadine Sugar FreeloratadineLoratadine 5 mg/5mLSolutionOralWalgreen Company0363-213100363-2131-08
Childrens Loratadine Sugar FreeloratadineLoratadine 5 mg/5mLSolutionOralSun Pharmaceutical Industries, Inc.51672-213151672-2131-0151672-2131-0451672-2131-08
Childrens Loratadine Sugar FreeloratadineLoratadine 5 mg/5mLSolutionOralH E B37808-13137808-0131-08
Childrens Loratadine Sugar FreeloratadineLoratadine 5 mg/5mLSolutionOralAmerican Sales Company41520-13141520-0131-08

Other NDCs under ANDA 201865

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

FDA NDC Directory listings under ANDA 201865
ProductStrengthForm · routeLabelerProduct NDC
Childrens AllergyloratadineLoratadine 5 mg/5mLSolutionOralCVS Pharmacy69842-535
LoratadineLoratadine 5 mg/5mLSolutionOralWALGREEN COMPANY0363-0771
Childrens AllergyloratadineLoratadine 5 mg/5mLSolutionOralWal-Mart Stores Inc49035-538
Childrens WalitinloratadineLoratadine 5 mg/5mLSolutionOralWalgreen Company0363-2108

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