What is NDC 70710-1151?

70710-1151 is the product NDC for Isosorbide dinitrate, Isosorbide dinitrate 30 mg/1 tablet, 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 Isosorbide dinitrate?

51 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Isosorbide dinitrate NDC 70710-1151

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-1151Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-1151Add 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
70710-1151-0	7071011510070710115100	1000 TABLET in 1 BOTTLE (70710-1151-0)Marketed from Nov 25, 2019
70710-1151-1	7071011510170710115101	100 TABLET in 1 BOTTLE (70710-1151-1)Marketed from Nov 25, 2019

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): Isosorbide dinitrate
Generic name (nonproprietary): isosorbide dinitrate
Active ingredients: Isosorbide dinitrate — 30 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Pharmaceuticals (USA) Inc.NDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213057
Marketing start: Nov 25, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 70710-1151_60a0c153-add8-44d9-a2f1-4c333d0eb42dSPL ID 60a0c153-add8-44d9-a2f1-4c333d0eb42dSPL set ID 16818b32-ee5e-4e07-b848-31e892c4b98aRxCUI 197839, 197840, 206842, 314055, 381056UNII IA7306519NUPC 0370710114916
Pharmacologic class: Nitrate Vasodilator

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

N470710115100 followed by a unit qualifier and the quantity

Package 70710-1151-00. 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 Aug 8, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Isosorbide dinitrate tablets are indicated for the prevention of angina pectoris due to coronary artery disease. The onset of action of immediate-release oral isosorbide dinitrate is not sufficiently rapid for this product to be useful in aborting an acute anginal episode.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70710-1151

What is NDC 70710-1151?: 70710-1151 is the product NDC for Isosorbide dinitrate, Isosorbide dinitrate 30 mg/1 tablet, 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?: Isosorbide dinitrate.
What is the active ingredient?: Isosorbide dinitrate.
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 Isosorbide dinitrate?: 51 other product NDCs are listed under this name. See all Isosorbide dinitrate 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 Isosorbide dinitrate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Isosorbide Dinitrate	Isosorbide dinitrate 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4405	70518-4405-00
Isosorbide dinitrate	Isosorbide dinitrate 30 mg/1	TabletOral	BluePoint Laboratories	68001-562	68001-0562-00
Isosorbide Dinitrate	Isosorbide dinitrate 10 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8463	00615-8463-39
Isosorbide Dinitrate	Isosorbide dinitrate 20 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8464	00615-8464-39
Isosorbide Dinitrate	Isosorbide dinitrate 30 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8465	00615-8465-39
Isosorbide Dinitrate	Isosorbide dinitrate 5 mg/1	TabletOral	Advagen Pharma Ltd	72888-081	72888-0081-0072888-0081-01
Isosorbide Dinitrate	Isosorbide dinitrate 10 mg/1	TabletOral	Advagen Pharma Ltd	72888-082	72888-0082-0072888-0082-01
Isosorbide Dinitrate	Isosorbide dinitrate 20 mg/1	TabletOral	Advagen Pharma Ltd	72888-083	72888-0083-0072888-0083-01
Isosorbide Dinitrate	Isosorbide dinitrate 30 mg/1	TabletOral	Advagen Pharma Ltd	72888-084	72888-0084-0072888-0084-01
Isosorbide Dinitrate	Isosorbide dinitrate 40 mg/1	TabletOral	Advagen Pharma Ltd	72888-085	72888-0085-0072888-0085-01

All 52 Isosorbide dinitrate NDCs

Other NDCs under ANDA 213057

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

FDA NDC Directory listings under ANDA 213057
Product	Strength	Form · route	Labeler	Product NDC
Isosorbide dinitrate	Isosorbide dinitrate 5 mg/1	TabletOral	Northstar Rx LLC	16714-007
Isosorbide dinitrate	Isosorbide dinitrate 10 mg/1	TabletOral	Northstar Rx LLC	16714-008
Isosorbide dinitrate	Isosorbide dinitrate 20 mg/1	TabletOral	Northstar Rx LLC	16714-009
Isosorbide dinitrate	Isosorbide dinitrate 30 mg/1	TabletOral	Northstar Rx LLC	16714-010
Isosorbide dinitrate	Isosorbide dinitrate 30 mg/1	TabletOral	BluePoint Laboratories	68001-562
Isosorbide dinitrate	Isosorbide dinitrate 5 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1148
Isosorbide dinitrate	Isosorbide dinitrate 10 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1149
Isosorbide dinitrate	Isosorbide dinitrate 20 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1150
Isosorbide dinitrate	Isosorbide dinitrate 40 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1152
Isosorbide dinitrate	Isosorbide dinitrate 5 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1501
Isosorbide dinitrate	Isosorbide dinitrate 10 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1502
Isosorbide dinitrate	Isosorbide dinitrate 20 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1503
Isosorbide dinitrate	Isosorbide dinitrate 30 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1504
Isosorbide dinitrate	Isosorbide dinitrate 40 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1505