What is NDC 71335-1183?

71335-1183 is the product NDC for Diclofenac Sodium and Misoprostol, Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1 tablet, delayed release, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, shown above in 10- and 11-digit form.

What is the active ingredient?

Diclofenac sodium, Misoprostol.

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 Diclofenac Sodium and Misoprostol?

10 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Diclofenac Sodium and Misoprostol NDC 71335-1183

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-1183Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-1183Add 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
71335-1183-1	7133511830171335118301	20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-1)Marketed from Jan 29, 2025
71335-1183-2	7133511830271335118302	14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-2)Marketed from Apr 10, 2019
71335-1183-3	7133511830371335118303	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-3)Marketed from Jan 29, 2025
71335-1183-4	7133511830471335118304	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-4)Marketed from Jan 29, 2025
71335-1183-5	7133511830571335118305	10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-5)Marketed from Jan 29, 2025

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): Diclofenac Sodium and Misoprostol
Generic name (nonproprietary): diclofenac sodium and misoprostol
Active ingredients: Diclofenac sodium — 75 mg/1Misoprostol — 200 ug/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203995
Marketing start: Dec 1, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)Synthetic (Chemical structure)
Identifiers: Product ID 71335-1183_3c1e7d73-b9c0-4260-87ed-049797c1e8dcSPL ID 3c1e7d73-b9c0-4260-87ed-049797c1e8dcSPL set ID d6671b66-00ad-4949-b51a-36e1130b1cb5RxCUI 1359105UNII QTG126297Q, 0E43V0BB57
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug; Prostaglandin E1 Analog

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

N471335118301 followed by a unit qualifier and the quantity

Package 71335-1183-01. 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 29, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Diclofenac sodium and misoprostol delayed-release tablets are indicated for treatment of the signs and symptoms of osteoarthritis or rheumatoid arthritis in adult patients at high risk of developing NSAID-induced gastric and duodenal ulcers and their complications. For a list of factors that may increase the risk of NSAID-induced gastric and duodenal ulcers and their complications [see Warnings and Precautions (5.3) ] . Diclofenac sodium and misoprostol delayed-release tablets are a combination of diclofenac sodium, a non-steroidal anti-inflammatory drug, and misoprostol, a prostaglandin-1 (PG E1) analog, indicated for the treatment of signs and symptoms of osteoarthritis or rheumatoid arthr…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1183

What is NDC 71335-1183?: 71335-1183 is the product NDC for Diclofenac Sodium and Misoprostol, Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1 tablet, delayed release, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Diclofenac Sodium and Misoprostol.
What is the active ingredient?: Diclofenac sodium, Misoprostol.
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 Diclofenac Sodium and Misoprostol?: 10 other product NDCs are listed under this name. See all Diclofenac Sodium and Misoprostol 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 Diclofenac Sodium and Misoprostol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Diclofenac Sodium and Misoprostol	Diclofenac sodium 50 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	Amneal Pharmaceuticals LLC	65162-436	65162-0436-0365162-0436-0665162-0436-09+1 more
Diclofenac Sodium and Misoprostol	Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	Amneal Pharmaceuticals LLC	65162-438	65162-0438-0365162-0438-0665162-0438-10
Diclofenac Sodium and Misoprostol	Diclofenac sodium 50 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	BluePoint Laboratories	68001-231	68001-0231-06
Diclofenac Sodium and Misoprostol	Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	BluePoint Laboratories	68001-232	68001-0232-06
Diclofenac Sodium and Misoprostol	Diclofenac sodium 50 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	AvKARE	42291-232	42291-0232-60
Diclofenac Sodium and Misoprostol	Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	AvKARE	42291-233	42291-0233-60
Diclofenac Sodium and Misoprostol	Diclofenac sodium 50 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	Actavis Pharma, Inc.	0591-0397	00591-0397-1900591-0397-60
Diclofenac Sodium and Misoprostol	Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	Actavis Pharma, Inc.	0591-0398	00591-0398-60
Diclofenac sodium and Misoprostol	Diclofenac sodium 50 mg/1; Misoprostol 200 ug/1	Tablet, Film coatedOral	Mylan Pharmaceuticals Inc.	59762-0028	59762-0028-0159762-0028-02
Diclofenac sodium and Misoprostol	Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1	Tablet, Film coatedOral	Mylan Pharmaceuticals Inc.	59762-0029	59762-0029-01

Other NDCs under ANDA 203995

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

FDA NDC Directory listings under ANDA 203995
Product	Strength	Form · route	Labeler	Product NDC
Diclofenac Sodium and Misoprostol	Diclofenac sodium 50 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	Amneal Pharmaceuticals LLC	65162-436
Diclofenac Sodium and Misoprostol	Diclofenac sodium 75 mg/1; Misoprostol 200 ug/1	Tablet, Delayed releaseOral	Amneal Pharmaceuticals LLC	65162-438