NDC codes

FDA NDC Directory
Product NDC (as listed)70377-033Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70377-0033Add 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 NDC11-digit (billing)PackageCopy
70377-033-11703770033117037700331130 TABLET, FILM COATED in 1 BOTTLE (70377-033-11)Marketed from Jul 17, 2025
70377-033-12703770033127037700331260 TABLET, FILM COATED in 1 BOTTLE (70377-033-12)Marketed from Jul 17, 2025
70377-033-137037700331370377003313180 TABLET, FILM COATED in 1 BOTTLE (70377-033-13)Marketed from Jul 17, 2025
70377-033-147037700331470377003314500 TABLET, FILM COATED in 1 BOTTLE (70377-033-14)Marketed from Jul 17, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Sacubitril and Valsartan
Generic name (nonproprietary)
sacubitril and valsartan
Active ingredients
Sacubitril — 97 mg/1Valsartan — 103 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Biocon Pharma Inc.NDC labeler code 70377
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213680
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)Neprilysin Inhibitors (Mechanism)
Identifiers
Product ID 70377-033_646f3b67-93b9-d084-fafc-40f726e960c2SPL ID 646f3b67-93b9-d084-fafc-40f726e960c2
Pharmacologic class
Angiotensin 2 Receptor Blocker; Neprilysin Inhibitor

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

N470377003311 followed by a unit qualifier and the quantity

Package 70377-0033-11. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70377-033

What is NDC 70377-033?
70377-033 is the product NDC for Sacubitril and Valsartan, Sacubitril 97 mg/1; Valsartan 103 mg/1 tablet, film coated, listed with the FDA by Biocon Pharma Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sacubitril and Valsartan.
What is the active ingredient?
Sacubitril, Valsartan.
Who is the labeler?
Biocon Pharma Inc., NDC labeler code 70377. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sacubitril and Valsartan?
89 other product NDCs are listed under this name. See all Sacubitril and 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 Sacubitril and Valsartan NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sacubitril and ValsartanSacubitril 49 mg/1; Valsartan 51 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-08284386-0082-1884386-0082-6084386-0082-78
Sacubitril and ValsartanSacubitril 24 mg/1; Valsartan 26 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-08184386-0081-1884386-0081-6084386-0081-78
Sacubitril and ValsartanSacubitril 97 mg/1; Valsartan 103 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-08384386-0083-1884386-0083-6084386-0083-78
Sacubitril and ValsartanSacubitril 97 mg/1; Valsartan 103 mg/1Tablet, Film coatedOralUmedica Laboratories USA Inc.60290-08760290-0087-0160290-0087-0260290-0087-03
Sacubitril and ValsartanSacubitril 24 mg/1; Valsartan 26 mg/1Tablet, Film coatedOralUmedica Laboratories USA Inc.60290-08560290-0085-0160290-0085-0260290-0085-03
Sacubitril and ValsartanSacubitril 49 mg/1; Valsartan 51 mg/1Tablet, Film coatedOralUmedica Laboratories USA Inc.60290-08660290-0086-0160290-0086-0260290-0086-03
Sacubitril and ValsartanSacubitril 24 mg/1; Valsartan 26 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-88072603-0880-0172603-0880-02
Sacubitril and ValsartanSacubitril 49 mg/1; Valsartan 51 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-88172603-0881-0172603-0881-02
Sacubitril and ValsartanSacubitril 97 mg/1; Valsartan 103 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-88272603-0882-0172603-0882-02
sacubitril and valsartanSacubitril 97 mg/1; Valsartan 103 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-93751407-0937-10

All 90 Sacubitril and Valsartan NDCs

Other NDCs under ANDA 213680

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

FDA NDC Directory listings under ANDA 213680
ProductStrengthForm · routeLabelerProduct NDC
Sacubitril and ValsartanSacubitril 24 mg/1; Valsartan 26 mg/1Tablet, Film coatedOralBiocon Pharma Inc.70377-031
Sacubitril and ValsartanSacubitril 49 mg/1; Valsartan 51 mg/1Tablet, Film coatedOralBiocon Pharma Inc.70377-032

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