What is NDC 70771-1885?

70771-1885 is the product NDC for Valsartan, Valsartan 320 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, 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 Valsartan?

131 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Valsartan NDC 70771-1885 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1885Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1885Add 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	Copy
70771-1885-9	70771188509	90 TABLET, FILM COATED in 1 BOTTLE (70771-1885-9)Marketed from Aug 30, 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): Valsartan
Generic name (nonproprietary): valsartan
Active ingredients: Valsartan — 320 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218991
Marketing start: Aug 30, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 70771-1885_a69225f3-d9ea-4ed4-b7ab-225147cad486SPL ID a69225f3-d9ea-4ed4-b7ab-225147cad486SPL set ID 1b60c816-7399-42c3-8b74-4dc9d82873ecRxCUI 349199, 349200, 349201, 349483UNII 80M03YXJ7IUPC 0372578134167
Pharmacologic class: Angiotensin 2 Receptor Blocker

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

N470771188509 followed by a unit qualifier and the quantity

Package 70771-1885-09. 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 23, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1885

What is NDC 70771-1885?: 70771-1885 is the product NDC for Valsartan, Valsartan 320 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Valsartan.
What is the active ingredient?: Valsartan.
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 Valsartan?: 131 other product NDCs are listed under this name. See all Valsartan 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 Valsartan NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
valsartan	Valsartan 320 mg/1	TabletOral	Jubilant Cadista Pharmaceuticals Inc.	59746-393	59746-0393-3059746-0393-3259746-0393-67+1 more
Valsartan	Valsartan 160 mg/1	Tablet, Film coatedOral	Laurus Labs Limited	42385-991	42385-0991-0542385-0991-3042385-0991-68+1 more
Valsartan	Valsartan 40 mg/1	Tablet, Film coatedOral	Laurus Labs Limited	42385-989	42385-0989-0542385-0989-3042385-0989-68
Valsartan	Valsartan 80 mg/1	Tablet, Film coatedOral	Laurus Labs Limited	42385-990	42385-0990-0542385-0990-3042385-0990-68+1 more
Valsartan	Valsartan 320 mg/1	Tablet, Film coatedOral	Laurus Labs Limited	42385-992	42385-0992-0542385-0992-3042385-0992-68+1 more
Valsartan	Valsartan 80 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1596	67046-1596-03
Valsartan	Valsartan 320 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1574	67046-1574-03
Valsartanvalsartan oral	Valsartan 4 mg/mL	SolutionOral	Advagen Pharma Ltd	72888-184	72888-0184-1372888-0184-48
Valsartan	Valsartan 40 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1882	70771-1882-03
Valsartan	Valsartan 80 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1883	70771-1883-09

All 132 Valsartan NDCs

Other NDCs under ANDA 218991

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

FDA NDC Directory listings under ANDA 218991
Product	Strength	Form · route	Labeler	Product NDC
Valsartan	Valsartan 80 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1883
Valsartan	Valsartan 40 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1882
Valsartan	Valsartan 160 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1884
Valsartan	Valsartan 40 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-553
Valsartan	Valsartan 320 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-134
Valsartan	Valsartan 40 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-131
Valsartan	Valsartan 80 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-132
Valsartan	Valsartan 160 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-133