What is NDC 71335-3010?

71335-3010 is the product NDC for Dexamethasone, Dexamethasone 1.5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dexamethasone NDC 71335-3010 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-3010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-3010Add 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 NDC	11-digit (billing)	Package
71335-3010-1	7133530100171335301001	35 TABLET in 1 BOTTLE (71335-3010-1)Marketed from Feb 4, 2026
71335-3010-2	7133530100271335301002	21 TABLET in 1 BOTTLE (71335-3010-2)Marketed from Feb 4, 2026
71335-3010-3	7133530100371335301003	51 TABLET in 1 BOTTLE (71335-3010-3)Marketed from Feb 4, 2026
71335-3010-4	7133530100471335301004	90 TABLET in 1 BOTTLE (71335-3010-4)Marketed from Feb 4, 2026
71335-3010-5	7133530100571335301005	120 TABLET in 1 BOTTLE (71335-3010-5)Marketed from Feb 4, 2026
71335-3010-6	7133530100671335301006	100 TABLET in 1 BOTTLE (71335-3010-6)Marketed from Feb 4, 2026
71335-3010-7	7133530100771335301007	55 TABLET in 1 BOTTLE (71335-3010-7)Marketed from Feb 4, 2026
71335-3010-8	7133530100871335301008	10 TABLET in 1 BOTTLE (71335-3010-8)Marketed from Feb 4, 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 — 1.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217695
Marketing start: Dec 5, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 71335-3010_320ac974-e60b-475f-afc7-9a52746e45c6SPL ID 320ac974-e60b-475f-afc7-9a52746e45c6SPL set ID b3217057-5945-452c-aa99-ab696fd8b5e7RxCUI 197580UNII 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

N471335301001 followed by a unit qualifier and the quantity

Package 71335-3010-01. 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 Feb 4, 2026.

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)

About NDC 71335-3010

What is NDC 71335-3010?: 71335-3010 is the product NDC for Dexamethasone, Dexamethasone 1.5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, 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 71335. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Dexamethasone	Dexamethasone 4 mg/1	TabletOral	Preferred Pharmaceuticals Inc	68788-4113	68788-4113-0168788-4113-0368788-4113-05+1 more
Dexamethasone	Dexamethasone .5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4669	70518-4669-00
Dexamethasone	Dexamethasone .25 mg/1	TabletOral	Pangea Pharmaceuticals, LLC	81279-117	81279-0117-60
Dexamethasone	Dexamethasone .5 mg/5mL	ElixirOral	ANI Pharmaceuticals, Inc.	70954-872	70954-0872-10
Dexamethasone	Dexamethasone 4 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-534	72789-0534-0172789-0534-2872789-0534-95
Dexamethasone	Dexamethasone .5 mg/5mL	ElixirOral	Bryant Ranch Prepack	72162-2600	72162-2600-02
Dexamethasone	Dexamethasone .5 mg/5mL	ElixirOral	Kanchan Healthcare Inc	85742-004	85742-0004-03
Dexamethasone	Dexamethasone 1.5 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3962	68071-3962-03
Dexamethasone	Dexamethasone .5 mg/1	TabletOral	Advagen Pharma Ltd.	72888-235	72888-0235-01
Dexamethasone	Dexamethasone .75 mg/1	TabletOral	Advagen Pharma Ltd.	72888-236	72888-0236-01

All 135 Dexamethasone NDCs

Other NDCs under ANDA 217695

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

FDA NDC Directory listings under ANDA 217695
Product	Strength	Form · route	Labeler	Product NDC
Dexamethasone	Dexamethasone 4 mg/1	TabletOral	Proficient Rx LP	82804-157
Dexamethasone	Dexamethasone 2 mg/1	TabletOral	Sportpharm LLC	85766-072
Dexamethasone	Dexamethasone .75 mg/1	TabletOral	Apotex Corp.	60505-6250
Dexamethasone	Dexamethasone .5 mg/1	TabletOral	Apotex Corp.	60505-6249
Dexamethasone	Dexamethasone 4 mg/1	TabletOral	Apotex Corp.	60505-6254
Dexamethasone	Dexamethasone 1 mg/1	TabletOral	Apotex Corp.	60505-6251
Dexamethasone	Dexamethasone 1.5 mg/1	TabletOral	Apotex Corp.	60505-6252
Dexamethasone	Dexamethasone 2 mg/1	TabletOral	Apotex Corp.	60505-6253
Dexamethasone	Dexamethasone 6 mg/1	TabletOral	Apotex Corp.	60505-6255