What is NDC 71335-1804?

71335-1804 is the product NDC for Celecoxib, Celecoxib 100 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 7 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 Celecoxib?

230 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Celecoxib NDC 71335-1804 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-1804Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-1804Add 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
71335-1804-1	7133518040171335180401	30 CAPSULE in 1 BOTTLE (71335-1804-1)Marketed from Apr 30, 2021
71335-1804-2	7133518040271335180402	20 CAPSULE in 1 BOTTLE (71335-1804-2)Marketed from Jan 30, 2025
71335-1804-3	7133518040371335180403	60 CAPSULE in 1 BOTTLE (71335-1804-3)Marketed from Mar 18, 2021
71335-1804-4	7133518040471335180404	90 CAPSULE in 1 BOTTLE (71335-1804-4)Marketed from Jul 28, 2022
71335-1804-5	7133518040571335180405	120 CAPSULE in 1 BOTTLE (71335-1804-5)Marketed from Jan 24, 2022
71335-1804-6	7133518040671335180406	14 CAPSULE in 1 BOTTLE (71335-1804-6)Marketed from Jan 30, 2025
71335-1804-7	7133518040771335180407	10 CAPSULE in 1 BOTTLE (71335-1804-7)Marketed from Jan 3, 2023

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): Celecoxib
Generic name (nonproprietary): celecoxib
Active ingredients: Celecoxib — 100 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204776
Marketing start: Jun 1, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 71335-1804_40e64c0a-b129-4059-8340-19a50b3278c0SPL ID 40e64c0a-b129-4059-8340-19a50b3278c0SPL set ID 550c828b-8c88-4c47-a7b8-a436aed46dc7RxCUI 205322UNII JCX84Q7J1L
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N471335180401 followed by a unit qualifier and the quantity

Package 71335-1804-01. 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 Jan 30, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Celecoxib is indicated Celecoxib is a nonsteroidal anti-inflammatory drug indicated for: Osteoarthritis (OA) ( 1.1 ) Rheumatoid Arthritis (RA) ( 1.2 ) Juvenile Rheumatoid Arthritis (JRA) in patients 2 years and older ( 1.3 ) Ankylosing Spondylitis (AS) ( 1.4 ) Acute Pain (AP) ( 1.5 ) Primary Dysmenorrhea (PD) ( 1.6 ) 1.1 Osteoarthritis (OA) For the management of the signs and symptoms of OA [see Clinical Studies (14.1) ] . 1.2 Rheumatoid Arthritis (RA) For the management of the signs and symptoms of RA [see Clinical Studies (14.2) ] . 1.3 Juvenile Rheumatoid Arthritis (JRA) For the management of the signs and symptoms of JRA in patients 2 years and older [see Clinical Studies (14.3) ] . 1.4 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1804

What is NDC 71335-1804?: 71335-1804 is the product NDC for Celecoxib, Celecoxib 100 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Celecoxib.
What is the active ingredient?: Celecoxib.
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 Celecoxib?: 230 other product NDCs are listed under this name. See all Celecoxib 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 Celecoxib NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	Direct_Rx	72189-695	72189-0695-3072189-0695-60
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	St. Mary's Medical Park Pharmacy	60760-942	60760-0942-60
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	Direct_Rx	72189-685	72189-0685-6072189-0685-72
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4726	70518-4726-00
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	St. Mary's Medical Park Pharmacy	60760-958	60760-0958-1560760-0958-3060760-0958-60
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0160	55154-0160-00
Celecoxib	Celecoxib 400 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4619	70518-4619-00
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	Major Pharmaceuticals	0904-7550	00904-7550-61
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	Major Pharmaceuticals	0904-7551	00904-7551-61
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	Avet Pharmaceuticals Inc.	23155-964	23155-0964-0123155-0964-05

All 231 Celecoxib NDCs

Other NDCs under ANDA 204776

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

FDA NDC Directory listings under ANDA 204776
Product	Strength	Form · route	Labeler	Product NDC
Celecoxib	Celecoxib 50 mg/1	CapsuleOral	Micro Labs Limited	42571-142
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	Micro Labs Limited	42571-143
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	Micro Labs Limited	42571-144
Celecoxib	Celecoxib 400 mg/1	CapsuleOral	Micro Labs Limited	42571-145
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	A-S Medication Solutions	50090-4789
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	A-S Medication Solutions	50090-6380
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-436
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-437
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	American Health Packaging	60687-436
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	American Health Packaging	60687-447
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-1066
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-2380
Celecoxib	Celecoxib 200 mg/1	CapsuleOral	Advanced Rx of Tennessee, LLC	80425-0040
Celecoxib	Celecoxib 100 mg/1	CapsuleOral	Proficient Rx LP	82804-151