NDC codes

FDA NDC Directory
Product NDC (as listed)51662-1367Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51662-1367Add 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
51662-1367-1516621367011 SYRINGE, GLASS in 1 BLISTER PACK (51662-1367-1) / 2 mL in 1 SYRINGE, GLASSMarketed from Oct 14, 2019

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/2mL
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091392
Marketing start
Listing expires
Other FDA classes
Dopamine D2 Antagonists (Mechanism)
Identifiers
Product ID 51662-1367_ef7bd5a0-02a8-7b66-e053-2995a90a8ffaSPL ID ef7bd5a0-02a8-7b66-e053-2995a90a8ffaSPL set ID 94e5acdf-f19c-749a-e053-2995a90ae451RxCUI 727619UNII W1792A2RVD
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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N451662136701 followed by a unit qualifier and the quantity

Package 51662-1367-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS & USAGE Diabetic Gastroparesis (Diabetic Gastric Stasis) Metoclopramide Injection (metoclopramide hydrochloride, USP) is indicated for the relief of symptoms associated with acute and recurrent diabetic gastric stasis. The Prevention of Nausea and Vomiting Associated with Emetogenic Cancer Chemotherapy Metoclopramide Injection is indicated for the prophylaxis of vomiting associated with emetogenic cancer chemotherapy. The Prevention of Postoperative Nausea and Vomiting Metoclopramide Injection is indicated for the prophylaxis of postoperative nausea and vomiting in those circumstances where nasogastric suction is undesirable. Small Bowel Intubation Metoclopramide Injection may be…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 091392

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

FDA NDC Directory listings under ANDA 091392
ProductStrengthForm · routeLabelerProduct NDC
Metoclopramidemetoclopramide hydrochlorideMetoclopramide hydrochloride 10 mg/2mLInjection, SolutionIntramuscular, IntravenousFresenius Kabi USA, LLC76045-101
Metoclopramidemetoclopramide hydrochlorideMetoclopramide hydrochloride 10 mg/2mLInjection, SolutionIntramuscular, IntravenousFresenius Kabi USA, LLC76045-213

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