What is NDC 70710-2158?

70710-2158 is the product NDC for Riociguat, Riociguat 1.5 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals USA Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

Zydus Pharmaceuticals USA Inc, NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Riociguat?

4 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Riociguat NDC 70710-2158 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-2158Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-2158Add 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
70710-2158-8	70710215808	9 TABLET, FILM COATED in 1 BOTTLE (70710-2158-8)Marketed from Sep 18, 2026
70710-2158-9	70710215809	90 TABLET, FILM COATED in 1 BOTTLE (70710-2158-9)Marketed from Sep 18, 2026

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): Riociguat
Generic name (nonproprietary): riociguat
Active ingredients: Riociguat — 1.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Pharmaceuticals USA IncNDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211135
Marketing start: Sep 18, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Guanylate Cyclase Stimulators (Mechanism)
Identifiers: Product ID 70710-2158_b7d9755e-0ea7-405a-90b5-95ae93e9c3b3SPL ID b7d9755e-0ea7-405a-90b5-95ae93e9c3b3
Pharmacologic class: Soluble Guanylate Cyclase Stimulator

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

N470710215808 followed by a unit qualifier and the quantity

Package 70710-2158-08. 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 70710-2158

What is NDC 70710-2158?: 70710-2158 is the product NDC for Riociguat, Riociguat 1.5 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals USA Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Riociguat.
What is the active ingredient?: Riociguat.
Who is the labeler?: Zydus Pharmaceuticals USA Inc, NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Riociguat?: 4 other product NDCs are listed under this name. See all Riociguat 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 Riociguat NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Riociguat	Riociguat .5 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2156	70710-2156-0870710-2156-09
Riociguat	Riociguat 1 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2157	70710-2157-0870710-2157-09
Riociguat	Riociguat 2 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2159	70710-2159-0870710-2159-09
Riociguat	Riociguat 2.5 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2160	70710-2160-0870710-2160-09

Other NDCs under ANDA 211135

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

FDA NDC Directory listings under ANDA 211135
Product	Strength	Form · route	Labeler	Product NDC
Riociguat	Riociguat .5 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2156
Riociguat	Riociguat 2.5 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2160
Riociguat	Riociguat 1 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2157
Riociguat	Riociguat 2 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc	70710-2159