NDC codes

FDA NDC Directory
Product NDC (as listed)71610-689Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0689Add 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
71610-689-307161006893030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-689-30)Marketed from Feb 1, 2023
71610-689-537161006895360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-689-53)Marketed from Feb 1, 2023
71610-689-607161006896090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-689-60)Marketed from Feb 1, 2023

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 — 30 mg/1
Dosage form
Tablet, Extended release
Route
Oral
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 71610-689_57e2138d-9144-44c7-926e-73810d632cecSPL ID 57e2138d-9144-44c7-926e-73810d632cecSPL set ID 75bb3a1f-3cb7-4450-8e59-27521a1ebc25RxCUI 198034UNII 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

N471610068930 followed by a unit qualifier and the quantity

Package 71610-0689-30. 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 .

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)

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 90 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-624
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 30 mg/1Tablet, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-841
NifedipineNifedipine 30 mg/1Tablet, Extended releaseOralIngenus Pharmaceuticals, LLC50742-620
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralIngenus Pharmaceuticals, LLC50742-621
NifedipineNifedipine 90 mg/1Tablet, Extended releaseOralIngenus Pharmaceuticals, LLC50742-622
NifedipineNifedipine 60 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC51655-780

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