Isosorbide Dinitrate NDC 0781-1695

NDC codes

FDA NDC Directory

Product NDC (as listed)0781-1695Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00781-1695Add 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
0781-1695-01	00781169501	100 TABLET in 1 BOTTLE (0781-1695-01)Marketed from Jan 7, 1988
0781-1695-10	00781169510	1000 TABLET in 1 BOTTLE (0781-1695-10)Marketed from Jan 7, 1988

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Isosorbide Dinitrate
Generic name (nonproprietary): isosorbide dinitrate
Active ingredients: Isosorbide dinitrate — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Sandoz Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 089367
Marketing start: Jan 7, 1988
Listing expires: Dec 31, 2026
Other FDA classes: Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 0781-1695_9c848a4f-2720-4c80-a0be-e49200cb10f9SPL ID 9c848a4f-2720-4c80-a0be-e49200cb10f9SPL set ID 71fdd147-a987-40b6-9f07-82d56525ceb8RxCUI 206842, 314055, 381056UNII IA7306519NUPC 0307811556017, 0307811695013, 0307811635019
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

N400781169501 followed by a unit qualifier and the quantity

Package 00781-1695-01. 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 Feb 1, 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.

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