What is NDC 71335-1989?

71335-1989 is the product NDC for Hydrocortisone, Hydrocortisone 5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 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 Hydrocortisone?

168 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Hydrocortisone NDC 71335-1989 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-1989Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-1989Add 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
71335-1989-1	7133519890171335198901	30 TABLET in 1 BOTTLE, PLASTIC (71335-1989-1)Marketed from Jul 18, 2024
71335-1989-2	7133519890271335198902	90 TABLET in 1 BOTTLE, PLASTIC (71335-1989-2)Marketed from Jul 18, 2024
71335-1989-3	7133519890371335198903	58 TABLET in 1 BOTTLE, PLASTIC (71335-1989-3)Marketed from Jul 18, 2024
71335-1989-4	7133519890471335198904	28 TABLET in 1 BOTTLE, PLASTIC (71335-1989-4)Marketed from Jul 18, 2024
71335-1989-5	7133519890571335198905	60 TABLET in 1 BOTTLE, PLASTIC (71335-1989-5)Marketed from Nov 11, 2021
71335-1989-6	7133519890671335198906	100 TABLET in 1 BOTTLE, PLASTIC (71335-1989-6)Marketed from Jul 18, 2024

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): Hydrocortisone
Generic name (nonproprietary): hydrocortisone
Active ingredients: Hydrocortisone — 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 040646
Marketing start: Mar 30, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 71335-1989_54e94095-73b5-4dfc-a0f7-1b97ea861f37SPL ID 54e94095-73b5-4dfc-a0f7-1b97ea861f37SPL set ID 47bfae62-bf25-413e-93fc-3c72c901f1a5RxCUI 197787UNII WI4X0X7BPJ
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

N471335198901 followed by a unit qualifier and the quantity

Package 71335-1989-01. 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 Jul 18, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hydrocortisone Tablets are indicated in the following conditions. 1. Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance) Congenital adrenal hyperplasia Non suppurative thyroiditis Hypercalcemia associated with cancer 2. Rheumatic Disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in: Psoriatic arthritis Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected c…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1989

What is NDC 71335-1989?: 71335-1989 is the product NDC for Hydrocortisone, Hydrocortisone 5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hydrocortisone.
What is the active ingredient?: Hydrocortisone.
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 Hydrocortisone?: 168 other product NDCs are listed under this name. See all Hydrocortisone 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 Hydrocortisone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Hydrocortisone	Hydrocortisone 1 g/100g	LotionTopical	Amazon.com Services LLC	72288-469	72288-0469-25
Hydrocortisone	Hydrocortisone 5 mg/1	TabletOral	Solco Healthcare LLC	43547-892	43547-0892-05
Hydrocortisone	Hydrocortisone 10 mg/1	TabletOral	Solco Healthcare LLC	43547-893	43547-0893-10
Hydrocortisone	Hydrocortisone 20 mg/1	TabletOral	Solco Healthcare LLC	43547-894	43547-0894-10
Hydrocortisone	Hydrocortisone 1 g/100g	CreamTopical	Amazon.com Services LLC	72288-713	72288-0713-64
Hydrocortisone	Hydrocortisone 25 mg/g	CreamTopical	Encube Ethicals, Inc.	21922-065	21922-0065-0521922-0065-30
Hydrocortisone	Hydrocortisone 20 mg/g	GelTopical	Redmont Pharmaceuticals, LLC	71741-455	71741-0455-31
Hydrocortisone	Hydrocortisone 10 mg/g	CreamTopical	Sportpharm LLC	85766-166	85766-0166-1085766-0166-25
hydrocortisone	Hydrocortisone 1 g/100g	CreamTopical	Sportpharm LLC	85766-151	85766-0151-28
Hydrocortisonehydrocortisone cream 1%	Hydrocortisone 1 g/100g	CreamTopical	Aldermed Inc.	87236-004	87236-0004-09

All 169 Hydrocortisone NDCs

Other NDCs under ANDA 040646

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

FDA NDC Directory listings under ANDA 040646
Product	Strength	Form · route	Labeler	Product NDC
Hydrocortisone	Hydrocortisone 5 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	0115-1696
Hydrocortisone	Hydrocortisone 10 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	0115-1697
Hydrocortisone	Hydrocortisone 20 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	0115-1700
Hydrocortisone	Hydrocortisone 10 mg/1	TabletOral	Major Pharmaceuticals	0904-7188
Hydrocortisone	Hydrocortisone 5 mg/1	TabletOral	AvPAK	50268-405
Hydrocortisone	Hydrocortisone 10 mg/1	TabletOral	AvPAK	50268-406
Hydrocortisone	Hydrocortisone 20 mg/1	TabletOral	AvPAK	50268-407
Hydrocortisone	Hydrocortisone 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8455
Hydrocortisone	Hydrocortisone 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2044
Hydrocortisone	Hydrocortisone 20 mg/1	TabletOral	Bryant Ranch Prepack	72162-2018