What is NDC 70771-1083?

70771-1083 is the product NDC for Diflunisal, Diflunisal 500 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 7 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Diflunisal?

4 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Diflunisal NDC 70771-1083 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1083Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1083Add 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
70771-1083-0	7077110830070771108300	1000 TABLET in 1 BOTTLE (70771-1083-0)Marketed from Sep 14, 2017
70771-1083-1	7077110830170771108301	100 TABLET in 1 BOTTLE (70771-1083-1)Marketed from Sep 14, 2017
70771-1083-3	7077110830370771108303	30 TABLET in 1 BOTTLE (70771-1083-3)Marketed from Sep 14, 2017
70771-1083-5	7077110830570771108305	500 TABLET in 1 BOTTLE (70771-1083-5)Marketed from Sep 14, 2017
70771-1083-6	7077110830670771108306	60 TABLET in 1 BOTTLE (70771-1083-6)Marketed from Sep 14, 2017
70771-1083-8	7077110830870771108308	10 BLISTER PACK in 1 CARTON (70771-1083-8) / 10 TABLET in 1 BLISTER PACKMarketed from Sep 14, 2017
70771-1083-9	7077110830970771108309	90 TABLET in 1 BOTTLE (70771-1083-9)Marketed from Sep 14, 2017

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): Diflunisal
Generic name (nonproprietary): diflunisal
Active ingredients: Diflunisal — 500 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203547
Marketing start: Sep 14, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 70771-1083_d5395b92-79af-436c-82ac-a6b70cd3b139SPL ID d5395b92-79af-436c-82ac-a6b70cd3b139SPL set ID d7a722be-4612-4b2e-827d-56fb5eef0aaeRxCUI 197603UNII 7C546U4DENUPC 0370771108312
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

N470771108300 followed by a unit qualifier and the quantity

Package 70771-1083-00. 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 Nov 22, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of diflunisal tablets and other treatment options before deciding to use diflunisal tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Diflunisal tablets are indicated for acute or long-term use for symptomatic treatment of the following: 1. Mild to moderate pain 2. Osteoarthritis 3. Rheumatoid arthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1083

What is NDC 70771-1083?: 70771-1083 is the product NDC for Diflunisal, Diflunisal 500 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Diflunisal.
What is the active ingredient?: Diflunisal.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diflunisal?: 4 other product NDCs are listed under this name. See all Diflunisal 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 Diflunisal NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Diflunisal	Diflunisal 500 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals USA, Inc.	0093-9222	00093-9222-0100093-9222-0500093-9222-06
Diflunisal	Diflunisal 500 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	68382-530	68382-0530-0168382-0530-0568382-0530-06+4 more
diflunisal	Diflunisal 500 mg/1	Tablet, Film coatedOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	14539-673	14539-0673-0114539-0673-0514539-0673-06
Diflunisal	Diflunisal 500 mg/1	Tablet, Film coatedOral	Chartwell RX, LLC	62135-456	62135-0456-60

Other NDCs under ANDA 203547

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

FDA NDC Directory listings under ANDA 203547
Product	Strength	Form · route	Labeler	Product NDC
Diflunisal	Diflunisal 500 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	68382-530