NDC codes

FDA NDC Directory
Product NDC (as listed)0143-1772Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00143-1772Add 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
0143-1772-0100143177201100 TABLET in 1 BOTTLE, PLASTIC (0143-1772-01)Marketed from Apr 26, 1983
0143-1772-10001431772101000 TABLET in 1 BOTTLE, PLASTIC (0143-1772-10)Marketed from Apr 26, 1983

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 dinitrate20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 088088
Marketing start
Listing expires
Other FDA classes
Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers
Product ID 0143-1772_9be99742-a98b-46d3-9447-81b45679fff9SPL ID 9be99742-a98b-46d3-9447-81b45679fff9SPL set ID f0b9b320-0bf8-4342-b654-135ccb6755c2RxCUI 206842, 314055, 381056UNII IA7306519NUPC 0301431769017, 0301431771010, 0301431772017
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

N400143177201 followed by a unit qualifier and the quantity

Package 00143-1772-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Isosorbide Dinitrate Tablets, USP 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)

Other NDCs under ANDA 088088

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

FDA NDC Directory listings under ANDA 088088
ProductStrengthForm · routeLabelerProduct NDC
Isosorbide DinitrateIsosorbide dinitrate 20 mg/1TabletOralCardinal Health 107, LLC55154-7991
Isosorbide DinitrateIsosorbide dinitrate 10 mg/1TabletOralCardinal Health 107, LLC55154-7990
Isosorbide DinitrateIsosorbide dinitrate 10 mg/1TabletOralGolden State Medical Supply, Inc.51407-148
Isosorbide DinitrateIsosorbide dinitrate 5 mg/1TabletOralGolden State Medical Supply, Inc.51407-147
Isosorbide DinitrateIsosorbide dinitrate 20 mg/1TabletOralGolden State Medical Supply, Inc.51407-149
Isosorbide DinitrateIsosorbide dinitrate 10 mg/1TabletOralMajor Pharmaceuticals0904-6619
Isosorbide DinitrateIsosorbide dinitrate 20 mg/1TabletOralMajor Pharmaceuticals0904-6620
Isosorbide DinitrateIsosorbide dinitrate 5 mg/1TabletOralHikma Pharmaceuticals USA Inc.0143-1769
Isosorbideisosorbide dinitrateIsosorbide dinitrate 20 mg/1TabletOralBluePoint Laboratories68001-375
Isosorbide DinitrateIsosorbide dinitrate 10 mg/1TabletOralHikma Pharmaceuticals USA Inc.0143-1771

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