NDC codes

FDA NDC Directory
Product NDC (as listed)50742-518Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50742-0518Add 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
50742-518-305074205183030 POUCH in 1 BOX, UNIT-DOSE (50742-518-30) / 1 PATCH in 1 POUCHMarketed from Dec 6, 2017

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)
Nitro-Dur
Generic name (nonproprietary)
nitroglycerin
Active ingredients
Nitroglycerin — 160 mg/1
Dosage form
Patch
Route
Transdermal
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 020145
Marketing start
Listing expires
Other FDA classes
Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers
Product ID 50742-518_fcec90fc-83c9-15e2-e053-6394a90ab2d5SPL ID fcec90fc-83c9-15e2-e053-6394a90ab2d5SPL set ID 5e15296c-5acd-4bcc-80a8-b49cb1ef3eb0RxCUI 486146, 486148, 486152, 861657, 899521, 899607, 899642, 899660, 899688, 899690, 899703, 899705UNII G59M7S0WS3
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. Transdermal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450742051830 followed by a unit qualifier and the quantity

Package 50742-0518-30. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Transdermal nitroglycerin is indicated for the prevention of angina pectoris due to coronary artery disease. The onset of action of transdermal nitroglycerin is not sufficiently rapid for this product to be useful in aborting an acute attack.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 020145

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

FDA NDC Directory listings under NDA 020145
ProductStrengthForm · routeLabelerProduct NDC
Nitroglycerin Transdermal Infusion SystemnitroglycerinNitroglycerin 120 mg/1PatchTransdermalDr. Reddy's Laboratories, Inc.43598-893
Nitroglycerin Transdermal Infusion SystemnitroglycerinNitroglycerin 80 mg/1PatchTransdermalDr. Reddy's Laboratories, Inc.43598-894
Nitroglycerin Transdermal Infusion SystemnitroglycerinNitroglycerin 40 mg/1PatchTransdermalDr. Reddy's Laboratories, Inc.43598-895
Nitroglycerin Transdermal Infusion SystemnitroglycerinNitroglycerin 20 mg/1PatchTransdermalDr. Reddy's Laboratories, Inc.43598-896
Nitro-DurnitroglycerinNitroglycerin 60 mg/1PatchTransdermalIngenus Pharmaceuticals, LLC50742-515
Nitro-DurnitroglycerinNitroglycerin 20 mg/1PatchTransdermalIngenus Pharmaceuticals, LLC50742-513
Nitro-DurnitroglycerinNitroglycerin 40 mg/1PatchTransdermalIngenus Pharmaceuticals, LLC50742-514
Nitro-DurnitroglycerinNitroglycerin 80 mg/1PatchTransdermalIngenus Pharmaceuticals, LLC50742-516
Nitro-DurnitroglycerinNitroglycerin 120 mg/1PatchTransdermalIngenus Pharmaceuticals, LLC50742-517

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