NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2157Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2157Add 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
67296-2157-16729621570110 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2157-1)Marketed from Mar 30, 2022

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)
Nifedipine
Generic name (nonproprietary)
nifedipine
Active ingredients
Nifedipine — 30 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216067
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 67296-2157_45d26939-fe46-b92b-e063-6294a90a64bbSPL ID 45d26939-fe46-b92b-e063-6294a90a64bbSPL set ID 32526983-f53a-fa68-e063-6394a90aa13fRxCUI 1812011UNII I9ZF7L6G2LUPC 0367877756905, 0367877757018, 0367877756059, 0367877758589
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

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

N467296215701 followed by a unit qualifier and the quantity

Package 67296-2157-01. 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 I. Vasospastic Angina Nifedipine extended-release tablets are indicated for the management of vasospastic angina confirmed by any of the following criteria: 1) classical pattern of angina at rest accompanied by ST segment elevation, 2) angina or coronary artery spasm provoked by ergonovine, or 3) angiographically demonstrated coronary artery spasm. In those patients who have had angiography, the presence of significant fixed obstructive disease is not incompatible with the diagnosis of vasospastic angina, provided that the above criteria are satisfied. Nifedipine extended-release tablets may also be used where the clinical presentation suggests a possible vasospastic comp…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 216067

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

FDA NDC Directory listings under ANDA 216067
ProductStrengthForm · routeLabelerProduct NDC
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralAscend Laboratories, LLC67877-757
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralAscend Laboratories, LLC67877-758
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6732
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6767
NifedipineNifedipine 90 mg/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-486
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-484
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-485
NifedipineNifedipine 90 mg/1Tablet, Extended releaseOralAscend Laboratories, LLC67877-756

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