NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4290Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4290Add 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
68071-4290-3680714290036807142900330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4290-3)Marketed from Feb 19, 2018
68071-4290-6680714290066807142900660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4290-6)Marketed from Feb 19, 2018
68071-4290-9680714290096807142900990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4290-9)Marketed from Feb 19, 2018

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 — 30 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075522
Marketing start
Listing expires
Other FDA classes
Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers
Product ID 68071-4290_1a3dc619-6b11-21b4-e063-6294a90acb1eSPL ID 1a3dc619-6b11-21b4-e063-6294a90acb1eSPL set ID 65935a15-a023-1941-e053-2991aa0a5eb4RxCUI 317110UNII LX1OH63030UPC 0368071429091
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

N468071429003 followed by a unit qualifier and the quantity

Package 68071-4290-03. 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 ISMN 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 68071-4290

What is NDC 68071-4290?
68071-4290 is the product NDC for Isosorbide Mononitrate, Isosorbide mononitrate 30 mg/1 tablet, extended release, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 3 package NDCs, 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?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 075522

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

FDA NDC Directory listings under ANDA 075522
ProductStrengthForm · routeLabelerProduct NDC
Isosorbide MononitrateIsosorbide mononitrate 30 mg/1Tablet, Extended releaseOralEdenbridge Pharmaceuticals LLC.42799-958
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralEdenbridge Pharmaceuticals LLC.42799-959
Isosorbide MononitrateIsosorbide mononitrate 30 mg/1Tablet, Extended releaseOralChartwell RX, LLC62135-586
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralChartwell RX, LLC62135-587
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralCoupler LLC67046-1632
Isosorbide MononitrateIsosorbide mononitrate 60 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2532

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