NDC codes

FDA NDC Directory
Product NDC (as listed)51662-1340Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51662-1340Add 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
51662-1340-1516621340015166213400130 g in 1 TUBE (51662-1340-1)Marketed from Dec 22, 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)
Nitroglycerin
Generic name (nonproprietary)
nitroglycerin
Active ingredients
Nitroglycerin — 20 mg/g
Dosage form
Ointment
Route
Topical
Labeler
HF Acquisition Co LLC, DBA HealthFirstNDC labeler code 51662
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 087355
Marketing start
Listing expires
Other FDA classes
Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers
Product ID 51662-1340_ef6d3da2-6bf9-fbc7-e053-2a95a90a74cdSPL ID ef6d3da2-6bf9-fbc7-e053-2a95a90a74cdSPL set ID 7da79fdf-0969-1ddd-e053-2991aa0a3ec4RxCUI 242946UNII 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451662134001 followed by a unit qualifier and the quantity

Package 51662-1340-01. 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 & USAGE Nitroglycerin ointment 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 anginal episode.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51662-1340

What is NDC 51662-1340?
51662-1340 is the product NDC for Nitroglycerin, Nitroglycerin 20 mg/g ointment, listed with the FDA by HF Acquisition Co LLC, DBA HealthFirst. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nitroglycerin.
What is the active ingredient?
Nitroglycerin.
Who is the labeler?
HF Acquisition Co LLC, DBA HealthFirst, NDC labeler code 51662. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nitroglycerin?
69 other product NDCs are listed under this name. See all Nitroglycerin 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 Nitroglycerin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NitroglycerinNitroglycerin 4 mg/gOintmentRectalPadagis Israel Pharmaceuticals Ltd45802-93245802-0932-94
NitroglycerinNitroglycerin 4 mg/gOintmentRectalBryant Ranch Prepack72162-264372162-2643-03
NitroglycerinNitroglycerin 4 mg/gOintmentRectalSolaris Pharma Corporation73473-50073473-0500-30
NitroglycerinNitroglycerin .3 mg/1TabletSublingualSolco Healthcare U.S., LLC43547-98543547-0985-0443547-0985-10
NitroglycerinNitroglycerin .4 mg/1TabletSublingualSolco Healthcare U.S., LLC43547-98643547-0986-0443547-0986-10
NitroglycerinNitroglycerin .6 mg/1TabletSublingualSolco Healthcare U.S., LLC43547-98743547-0987-0443547-0987-10
NitroglycerinNitroglycerin 20 mg/gOintmentTopicalEncube Ethicals, Inc.21922-05421922-0054-0521922-0054-47
nitroglycerinNitroglycerin .4 mg/1TabletSublingualREMEDYREPACK INC.70518-427770518-4277-0070518-4277-01
NitroglycerinNitroglycerin 4 mg/gOintmentRectalEncube Ethicals, Inc.21922-04821922-0048-05
NitroglycerinNitroglycerin 400 ug/1SprayOralHF Acquisition Co LLC, DBA HealthFirst51662-167251662-1672-01

All 70 Nitroglycerin NDCs

Other NDCs under ANDA 087355

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

FDA NDC Directory listings under ANDA 087355
ProductStrengthForm · routeLabelerProduct NDC
Nitro-BidnitroglycerinNitroglycerin 20 mg/gOintmentTopicalSavage Laboratories a division of Fougera Pharmaceuticals, LLC0281-0326

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