NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2600Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2600Add 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
72162-2600-27216226000272162260002237 mL in 1 BOTTLE (72162-2600-2)Marketed from Jan 9, 2026

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)
Dexamethasone
Generic name (nonproprietary)
dexamethasone
Active ingredients
Dexamethasone — .5 mg/5mL
Dosage form
Elixir
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 084754
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72162-2600_5ea02dfb-2164-44a3-b106-dd3bdec8fa09SPL ID 5ea02dfb-2164-44a3-b106-dd3bdec8fa09SPL set ID 075717e3-be2a-4bb3-bead-492761bfb287RxCUI 309686UNII 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

N472162260002 followed by a unit qualifier and the quantity

Package 72162-2600-02. 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: Atopic dermatitis, Bronchial asthma, Contact dermatitis, Drug hypersensitivity reactions, Seasonal or perennial allergic rhinitis, and Serum sickness. Collagen Diseases During an exacerbation or as maintenance therapy in selected cases of: Systemic lupus erythematosus, and Acute rheumatic carditis. Dermatologic Diseases Bullous dermatitis herpetiformis, Exfoliative dermatitis, Mycosis fungoides, Pemphigus, Severe erythema multiforme (Stevens-Johnson syndrome), Severe psoriasis, and Severe seborrheic dermatitis. Edematous States To induce a di…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2600

What is NDC 72162-2600?
72162-2600 is the product NDC for Dexamethasone, Dexamethasone .5 mg/5mL elixir, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dexamethasone.
What is the active ingredient?
Dexamethasone.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dexamethasone?
134 other product NDCs are listed under this name. See all Dexamethasone 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 Dexamethasone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DexamethasoneDexamethasone 4 mg/1TabletOralPreferred Pharmaceuticals Inc68788-411368788-4113-0168788-4113-0368788-4113-05+1 more
DexamethasoneDexamethasone .5 mg/1TabletOralREMEDYREPACK INC.70518-466970518-4669-00
DexamethasoneDexamethasone .25 mg/1TabletOralPangea Pharmaceuticals, LLC81279-11781279-0117-60
DexamethasoneDexamethasone .5 mg/5mLElixirOralANI Pharmaceuticals, Inc.70954-87270954-0872-10
DexamethasoneDexamethasone 4 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-53472789-0534-0172789-0534-2872789-0534-95
DexamethasoneDexamethasone .5 mg/5mLElixirOralKanchan Healthcare Inc85742-00485742-0004-03
DexamethasoneDexamethasone 1.5 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-396268071-3962-03
DexamethasoneDexamethasone .5 mg/1TabletOralAdvagen Pharma Ltd.72888-23572888-0235-01
DexamethasoneDexamethasone .75 mg/1TabletOralAdvagen Pharma Ltd.72888-23672888-0236-01
DexamethasoneDexamethasone 1 mg/1TabletOralAdvagen Pharma Ltd.72888-23772888-0237-01

All 135 Dexamethasone NDCs

Other NDCs under ANDA 084754

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

FDA NDC Directory listings under ANDA 084754
ProductStrengthForm · routeLabelerProduct NDC
DexamethasoneDexamethasone .5 mg/5mLElixirOralMarlex Pharmaceuticals, Inc10135-795
DexamethasoneDexamethasone .5 mg/5mLElixirOralANI Pharmaceuticals, Inc.70954-872
DexamethasoneDexamethasone .5 mg/5mLElixirOralKesin Pharma Corporation81033-010
DexamethasoneDexamethasone .5 mg/5mLElixirOralKanchan Healthcare Inc85742-004

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