NDC codes

FDA NDC Directory
Product NDC (as listed)55154-7292Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55154-7292Add 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
55154-7292-0551547292005515472920010 BLISTER PACK in 1 BAG (55154-7292-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Jan 5, 2015

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 Mononitrate
Generic name (nonproprietary)
isosorbide mononitrate
Active ingredients
Isosorbide mononitrate — 60 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Cardinal Health 107, LLCNDC labeler code 55154
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200495
Marketing start
Listing expires
Other FDA classes
Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers
Product ID 55154-7292_1e850741-a971-40d6-9c70-dfdcc9d549d7SPL ID 1e850741-a971-40d6-9c70-dfdcc9d549d7SPL set ID 72b8a20c-5833-4765-a4b5-9066eaec6ea1RxCUI 317110, 353538UNII LX1OH63030UPC 0055154729109, 0055154729208
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

N455154729200 followed by a unit qualifier and the quantity

Package 55154-7292-00. 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 mononitrate extended-release tablets, USP are indicated for the prevention of angina pectoris due to coronary artery disease. The onset of action of oral isosorbide mononitrate 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 55154-7292

What is NDC 55154-7292?
55154-7292 is the product NDC for Isosorbide Mononitrate, Isosorbide mononitrate 60 mg/1 tablet, extended release, listed with the FDA by Cardinal Health 107, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Isosorbide Mononitrate.
What is the active ingredient?
Isosorbide mononitrate.
Who is the labeler?
Cardinal Health 107, LLC, NDC labeler code 55154. 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 Mononitrate?
61 other product NDCs are listed under this name. See all Isosorbide Mononitrate 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 Mononitrate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Isosorbide MononitrateIsosorbide mononitrate 120 mg/1Tablet, Extended releaseOralAiPing Pharmaceutical, Inc.11788-16111788-0161-01
Isosorbide MononitrateIsosorbide mononitrate 30 mg/1Tablet, Extended releaseOralAiPing Pharmaceutical, Inc.11788-15911788-0159-0111788-0159-0511788-0159-10
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralAiPing Pharmaceutical, Inc.11788-16011788-0160-0111788-0160-0511788-0160-10
Isosorbide MononitrateIsosorbide mononitrate 10 mg/1TabletOralCoupler LLC67046-168767046-1687-03
Isosorbide MononitrateIsosorbide mononitrate 20 mg/1TabletOralGenus Lifesciences Inc.64950-25164950-0251-01
Isosorbide MononitrateIsosorbide mononitrate 10 mg/1TabletOralGenus Lifesciences Inc.64950-25064950-0250-01
Isosorbide MononitrateIsosorbide mononitrate 10 mg/1TabletOralANI Pharmaceuticals, Inc.62559-25262559-0252-01
Isosorbide MononitrateIsosorbide mononitrate 20 mg/1TabletOralANI Pharmaceuticals, Inc.62559-25362559-0253-01
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralCoupler LLC67046-163267046-1632-03
isosorbide mononitrateIsosorbide mononitrate 20 mg/1TabletOralCoupler LLC67046-157867046-1578-03

All 62 Isosorbide Mononitrate NDCs

Other NDCs under ANDA 200495

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

FDA NDC Directory listings under ANDA 200495
ProductStrengthForm · routeLabelerProduct NDC
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralNCS HealthCare of KY, LLC dba Vangard Labs0615-7768
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralMajor Pharmaceuticals0904-6450
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralTorrent Pharmaceuticals Limited13668-105
Isosorbide MononitrateIsosorbide mononitrate 120 mg/1Tablet, Extended releaseOralTorrent Pharmaceuticals Limited13668-106
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralAmerican Health Packaging60687-794

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