NDC codes

FDA NDC Directory
Product NDC (as listed)50742-621Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50742-0621Add 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
50742-621-015074206210150742062101100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-621-01)Marketed from Feb 15, 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)
Nifedipine
Generic name (nonproprietary)
nifedipine
Active ingredients
Nifedipine — 60 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Ingenus Pharmaceuticals, LLCNDC labeler code 50742
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202987
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 50742-621_182d5c87-db57-4042-a1e8-d2c78b07789bSPL ID 182d5c87-db57-4042-a1e8-d2c78b07789bSPL set ID 4d02eba2-e964-4fa7-aaae-25949b5f0316RxCUI 198034, 198035, 198036UNII I9ZF7L6G2L
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

N450742062101 followed by a unit qualifier and the quantity

Package 50742-0621-01. 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 AND USAGE Nifedipine extended-release tablets, USP are indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive agents.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50742-621

What is NDC 50742-621?
50742-621 is the product NDC for Nifedipine, Nifedipine 60 mg/1 tablet, extended release, listed with the FDA by Ingenus Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nifedipine.
What is the active ingredient?
Nifedipine.
Who is the labeler?
Ingenus Pharmaceuticals, LLC, NDC labeler code 50742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nifedipine?
127 other product NDCs are listed under this name. See all Nifedipine 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 Nifedipine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NifedipineNifedipine 30 mg/1Tablet, Film coated, Extended releaseOralCoupler LLC67046-026067046-0260-03
NifedipineNifedipine 10 mg/1CapsuleOralREMEDYREPACK INC.70518-462570518-4625-00
NifedipineNifedipine 10 mg/1CapsuleOralCardinal Health 107, LLC55154-019655154-0196-00
NifedipineNifedipine 90 mg/1Tablet, Film coated, Extended releaseOralSt. Mary's Medical Park Pharmacy60760-86260760-0862-90
NifedipineNifedipine 60 mg/1Tablet, Film coated, Extended releaseOralSt. Mary's Medical Park Pharmacy60760-85960760-0859-90
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC51655-38651655-0386-52
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC51655-59351655-0593-26
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralAlembic Pharmaceuticals Limited46708-73246708-0732-3146708-0732-6346708-0732-91
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralAlembic Pharmaceuticals Limited46708-73346708-0733-3146708-0733-63
NifedipineNifedipine 90 mg/1Tablet, Extended releaseOralAlembic Pharmaceuticals Limited46708-73446708-0734-31

All 128 Nifedipine NDCs

Other NDCs under ANDA 202987

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

FDA NDC Directory listings under ANDA 202987
ProductStrengthForm · routeLabelerProduct NDC
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralIngenus Pharmaceuticals, LLC50742-620
NifedipineNifedipine 90 mg/1Tablet, Extended releaseOralIngenus Pharmaceuticals, LLC50742-622
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-622
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-623
NifedipineNifedipine 90 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-624
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC51655-780
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-689
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-841

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