NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4650Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4650Add 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
70518-4650-07051846500050 POUCH in 1 BOX (70518-4650-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4650-1)Marketed from Apr 29, 2026

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)
Dipyridamole
Generic name (nonproprietary)
dipyridamole
Active ingredients
Dipyridamole — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040874
Marketing start
Listing expires
Other FDA classes
Decreased Platelet Aggregation (Physiologic effect)
Identifiers
Product ID 70518-4650_509b6d30-eda6-417e-e063-6294a90a4a94SPL ID 509b6d30-eda6-417e-e063-6294a90a4a94SPL set ID 226099e2-70bb-4b9b-bb52-c20fbca2aec5RxCUI 197622UNII 64ALC7F90C
Pharmacologic class
Platelet Aggregation Inhibitor

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

N470518465000 followed by a unit qualifier and the quantity

Package 70518-4650-00. 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 Dipyridamole tablets are indicated as an adjunct to coumarin anticoagulants in the prevention of postoperative thromboembolic complications of cardiac valve replacement.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040874

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

FDA NDC Directory listings under ANDA 040874
ProductStrengthForm · routeLabelerProduct NDC
DipyridamoleDipyridamole 50 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-663
DipyridamoleDipyridamole 25 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-662
DipyridamoleDipyridamole 75 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-664
DipyridamoleDipyridamole 25 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-187
DipyridamoleDipyridamole 50 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-188
DipyridamoleDipyridamole 75 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-189

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in