NDC codes

FDA NDC Directory
Product NDC (as listed)87717-001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87717-0001Add 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
87717-001-018771700010187717000101100 TABLET in 1 BOTTLE (87717-001-01)Marketed from Aug 27, 2026
87717-001-028771700010287717000102500 TABLET in 1 BOTTLE (87717-001-02)Marketed from Aug 27, 2026

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)
Desloratadine
Generic name (nonproprietary)
desloratadine
Active ingredients
Desloratadine — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Morepen Bio Inc.NDC labeler code 87717
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078355
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 87717-001_59f13ac4-d82e-d19d-e063-6394a90ac603SPL ID 59f13ac4-d82e-d19d-e063-6394a90ac603SPL set ID 21174c0f-9204-4c75-b6e6-2f9ada5b535dRxCUI 349420UNII FVF865388RUPC 0387717001026, 0387717001019
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 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

N487717000101 followed by a unit qualifier and the quantity

Package 87717-0001-01. 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)

Desloratadine Tablets are a histamine-1 (H1) receptor antagonist indicated for: Seasonal Allergic Rhinitis: relief of nasal and non-nasal symptoms in patients 12 years of age and older. ( 1.1 ) Perennial Allergic Rhinitis: relief of nasal and non-nasal symptoms in patients 12 years of age and older. ( 1.2 ) Chronic Idiopathic Urticaria: symptomatic relief of pruritus, reduction in the number of hives, and size of hives in patients 12 years of age and older. ( 1.3 ) 1.1 Seasonal Allergic Rhinitis Desloratadine Tablets are indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis in patients 12 years of age and older. 1.2 Perennial Allergic Rhinitis Desloratadi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87717-001

What is NDC 87717-001?
87717-001 is the product NDC for Desloratadine, Desloratadine 5 mg/1 tablet, listed with the FDA by Morepen Bio Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Desloratadine.
What is the active ingredient?
Desloratadine.
Who is the labeler?
Morepen Bio Inc., NDC labeler code 87717. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Desloratadine?
11 other product NDCs are listed under this name. See all Desloratadine 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 Desloratadine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DesloratadineDesloratadine 5 mg/1Tablet, Film coatedOralNatco Pharma USA LLC69339-19469339-0194-0169339-0194-05
DesloratadineDesloratadine 5 mg/1Tablet, Film coatedOralBionpharma Inc.69452-36369452-0363-2069452-0363-30
DesloratadineDesloratadine 5 mg/1TabletOralA-S Medication Solutions50090-397550090-3975-0050090-3975-01
DesloratadineDesloratadine 5 mg/1TabletOralVirtus Pharmaceuticals, LLC69543-10769543-0107-1069543-0107-50
DesloratadineDesloratadine 5 mg/1TabletOralBryant Ranch Prepack72162-230872162-2308-0172162-2308-0372162-2308-05
DesloratadineDesloratadine 5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-479450090-4794-00
DesloratadineDesloratadine 5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-672450090-6724-00
DesloratadineDesloratadine 5 mg/1Tablet, Film coatedOralLupin Pharmaceuticals, Inc.68180-15368180-0153-0168180-0153-02
DesloratadineDesloratadine 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-100071335-1000-0171335-1000-0271335-1000-03
DesloratadineDesloratadine 5 mg/1Tablet, Orally disintegratingOralDr. Reddy's Laboratories Limited55111-36055111-0360-0655111-0360-31

All 12 Desloratadine NDCs

Other NDCs under ANDA 078355

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

FDA NDC Directory listings under ANDA 078355
ProductStrengthForm · routeLabelerProduct NDC
DesloratadineDesloratadine 5 mg/1TabletOralA-S Medication Solutions50090-3975
DesloratadineDesloratadine 5 mg/1TabletOralVirtus Pharmaceuticals, LLC69543-107
DesloratadineDesloratadine 5 mg/1TabletOralBryant Ranch Prepack72162-2308

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