NDC codes

FDA NDC Directory
Product NDC (as listed)43063-266Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43063-0266Add 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
43063-266-07430630266077 TABLET in 1 BOTTLE, PLASTIC (43063-266-07)Marketed from Aug 3, 2010

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)
Dexamethasone
Generic name (nonproprietary)
dexamethasone
Active ingredients
Dexamethasone — 2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 087916
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 43063-266_4137927a-c11c-b316-e063-6294a90a7ca7SPL ID 4137927a-c11c-b316-e063-6294a90a7ca7SPL set ID 2ceb3a01-f5bb-4538-b5c1-cea400901d02RxCUI 197581UNII 7S5I7G3JQL
Pharmacologic class
Corticosteroid

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

N443063026607 followed by a unit qualifier and the quantity

Package 43063-0266-07. 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)

INDICATIONS AND USAGE Allergic States Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, and serum sickness. Dermatologic Diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, and severe erythema multiforme (Stevens-Johnson syndrome). Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; may be used in conjunction with synthetic mineralocorticoid analogs where applicable; in infancy mineralocortico…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 087916

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

FDA NDC Directory listings under ANDA 087916
ProductStrengthForm · routeLabelerProduct NDC
DexamethasoneDexamethasone 2 mg/1TabletOralProficient Rx LP63187-383
DexamethasoneDexamethasone 2 mg/1TabletOralCardinal Health 107, LLC55154-4914
DexamethasoneDexamethasone 2 mg/1TabletOralDoc Rx69306-112

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