NDC codes

FDA NDC Directory
Product NDC (as listed)72888-082Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72888-0082Add 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
72888-082-00728880082001000 TABLET in 1 BOTTLE (72888-082-00)Marketed from Jul 8, 2022
72888-082-0172888008201100 TABLET in 1 BOTTLE (72888-082-01)Marketed from Jul 8, 2022

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)
Isosorbide Dinitrate
Generic name (nonproprietary)
isosorbide dinitrate
Active ingredients
Isosorbide dinitrate10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215723
Marketing start
Listing expires
Other FDA classes
Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers
Product ID 72888-082_47a16566-2f2d-7df8-e063-6394a90a9012SPL ID 47a16566-2f2d-7df8-e063-6394a90a9012SPL set ID b166eb5b-bad8-4663-9c05-1c43539dab2cRxCUI 197839, 197840, 206842, 314055, 381056UNII IA7306519NUPC 0372888082004, 0372888083001, 0372888084008, 0372888081007, 0372888082011, 0372888081014, 0372888083018, 0372888084015, 0372888085005, 0372888085012
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

N472888008200 followed by a unit qualifier and the quantity

Package 72888-0082-00. 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 .

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)

Other NDCs under ANDA 215723

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

FDA NDC Directory listings under ANDA 215723
ProductStrengthForm · routeLabelerProduct NDC
Isosorbide DinitrateIsosorbide dinitrate 10 mg/1TabletOralProficient Rx LP82804-117
Isosorbide DinitrateIsosorbide dinitrate 5 mg/1TabletOralAdvagen Pharma Ltd72888-081
Isosorbide DinitrateIsosorbide dinitrate 40 mg/1TabletOralAdvagen Pharma Ltd72888-085
Isosorbide DinitrateIsosorbide dinitrate 20 mg/1TabletOralAdvagen Pharma Ltd72888-083
Isosorbide DinitrateIsosorbide dinitrate 30 mg/1TabletOralAdvagen Pharma Ltd72888-084
Isosorbide DinitrateIsosorbide dinitrate 10 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8463
Isosorbide DinitrateIsosorbide dinitrate 20 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8464
Isosorbide DinitrateIsosorbide dinitrate 10 mg/1TabletOralREMEDYREPACK INC.70518-4405
Isosorbide DinitrateIsosorbide dinitrate 30 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8465
Isosorbide DinitrateIsosorbide dinitrate 20 mg/1TabletOralProficient Rx LP82804-108

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