NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4541Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4541Add 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
70518-4541-07051845410040 TABLET in 1 BOTTLE, PLASTIC (70518-4541-0)Marketed from Dec 23, 2025

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)
Metoclopramide
Generic name (nonproprietary)
metoclopramide
Active ingredients
Metoclopramide hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 017854
Marketing start
Marketing end
Other FDA classes
Dopamine D2 Antagonists (Mechanism)
Identifiers
Product ID 70518-4541_5b9c4cff-c1e4-1ddf-e063-6294a90a5b51SPL ID 5b9c4cff-c1e4-1ddf-e063-6294a90a5b51
Pharmacologic class
Dopamine-2 Receptor Antagonist

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

N470518454100 followed by a unit qualifier and the quantity

Package 70518-4541-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under NDA 017854

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

FDA NDC Directory listings under NDA 017854
ProductStrengthForm · routeLabelerProduct NDC
Reglanmetoclopramide hydrochlorideMetoclopramide hydrochloride 10 mg/1TabletOralANI Pharmaceuticals, Inc.62559-166
Reglanmetoclopramide hydrochlorideMetoclopramide hydrochloride 5 mg/1TabletOralANI Pharmaceuticals, Inc.62559-165
MetoclopramideMetoclopramide hydrochloride 5 mg/1TabletOralANI Pharmaceuticals, Inc.62559-295
MetoclopramideMetoclopramide hydrochloride 10 mg/1TabletOralANI Pharmaceuticals, Inc.62559-296
MetoclopramideMetoclopramide hydrochloride 5 mg/1TabletOralRedpharm Drug67296-2213

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