What is NDC 50090-0132?

50090-0132 is the product NDC for Metoclopramide, Metoclopramide hydrochloride 10 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Metoclopramide?

71 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Metoclopramide NDC 50090-0132 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-0132Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-0132Add 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 NDC	11-digit (billing)	Package	Copy
50090-0132-0	5009001320050090013200	30 TABLET in 1 BOTTLE (50090-0132-0)Marketed from Nov 28, 2014

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
Labeler: A-S Medication SolutionsNDC labeler code 50090
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070184
Marketing start: Sep 30, 1990
Listing expires: Dec 31, 2026
Other FDA classes: Dopamine D2 Antagonists (Mechanism)
Identifiers: Product ID 50090-0132_f422f5a9-22c0-44e4-8645-7280afca8e15SPL ID f422f5a9-22c0-44e4-8645-7280afca8e15SPL set ID 264c4f48-51f4-458f-9e61-1adafdf604fcRxCUI 311666UNII 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 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

N450090013200 followed by a unit qualifier and the quantity

Package 50090-0132-00. 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 Feb 4, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

Metoclopramide tablets are indicated for the: Treatment for 4 to 12 weeks of symptomatic, documented gastroesophageal reflux in adults who fail to respond to conventional therapy. Relief of symptoms in adults with acute and recurrent diabetic gastroparesis. Limitations of Use : Metoclopramide tablets are not recommended for use in pediatric patients due to the risk of developing tardive dyskinesia (TD) and other extrapyramidal symptoms as well as the risk of methemoglobinemia in neonates [ see Use in Specific Populations ( 8.4 ) ]. Metoclopramide tablets are indicated for the: Treatment for 4 to 12 weeks of symptomatic, documented gastroesophageal reflux in adults who fail to respond to conv…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-0132

What is NDC 50090-0132?: 50090-0132 is the product NDC for Metoclopramide, Metoclopramide hydrochloride 10 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Metoclopramide.
What is the active ingredient?: Metoclopramide hydrochloride.
Who is the labeler?: A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Metoclopramide?: 71 other product NDCs are listed under this name. See all Metoclopramide 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 Metoclopramide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Metoclopramide	Metoclopramide hydrochloride 5 mg/mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	36000-366	36000-0366-25
Metoclopramide	Metoclopramide hydrochloride 5 mg/1	TabletOral	Coupler LLC	67046-0186	67046-0186-03
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Coupler LLC	67046-0581	67046-0581-03
Metoclopramidemetoclopramide hydrochloride	Metoclopramide hydrochloride 5 mg/mL	InjectionIntramuscular, Intravenous	Henry Schein, Inc.	0404-9771	00404-9771-02
Metoclopramide	Metoclopramide hydrochloride 5 mg/1	TabletOral	Safecor Health LLC	48433-066	48433-0066-20
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Safecor Health LLC	48433-067	48433-0067-20
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4541	70518-4541-00
Metoclopramide	Metoclopramide hydrochloride 5 mg/mL	Injection, SolutionIntramuscular, Intravenous	Cardinal Health 107, LLC	55154-7832	55154-7832-05
Metoclopramide	Metoclopramide hydrochloride 5 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc.	50228-232	50228-0232-0150228-0232-05
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc.	50228-233	50228-0233-0150228-0233-0550228-0233-10

All 72 Metoclopramide NDCs

Other NDCs under ANDA 070184

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

FDA NDC Directory listings under ANDA 070184
Product	Strength	Form · route	Labeler	Product NDC
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7930
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	66267-827
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Mylan Institutional Inc.	51079-888
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	53401-027
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	AvKARE	42291-596
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Proficient Rx LP	63187-235
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-0669
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Coupler LLC	67046-0581
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	American Health Packaging	60687-631
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-1193
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-0362
Metoclopramide	Metoclopramide hydrochloride 5 mg/1	TabletOral	Proficient Rx LP	63187-404
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Safecor Health LLC	48433-067
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Northwind Health Company, LLC	51655-240
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-2203
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8285
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-8745
Metoclopramide	Metoclopramide hydrochloride 10 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-286