What is NDC 0143-9873?

0143-9873 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 5 mg/5mL injection, solution, listed with the FDA by Hikma Pharmaceuticals USA Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Hikma Pharmaceuticals USA Inc., NDC labeler code 0143. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Metoprolol Tartrate?

224 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Metoprolol Tartrate NDC 0143-9873 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0143-9873Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00143-9873Add 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
0143-9873-10	0014398731000143987310	5 mL in 1 VIAL (0143-9873-10)Marketed from May 30, 2007
0143-9873-25	0014398732500143987325	25 VIAL in 1 CARTON (0143-9873-25) / 5 mL in 1 VIAL (0143-9873-10)Marketed from May 30, 2007

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Metoprolol Tartrate
Generic name (nonproprietary): metoprolol tartrate
Active ingredients: Metoprolol tartrate — 5 mg/5mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Hikma Pharmaceuticals USA Inc.NDC labeler code 0143
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077761
Marketing start: May 30, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 0143-9873_6a34f3f1-4b17-4864-97ec-405fffb45f20SPL ID 6a34f3f1-4b17-4864-97ec-405fffb45f20SPL set ID c7ec36bb-bc6f-42de-9974-a50ac13e9410RxCUI 866508UNII W5S57Y3A5L
Pharmacologic class: beta-Adrenergic 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 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

N400143987310 followed by a unit qualifier and the quantity

Package 00143-9873-10. 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 Mar 26, 2025.

Indications (excerpt from the label)

Metoprolol Tartrate Injection, USP is indicated in the treatment of definite or suspected acute myocardial infarction in hemodynamically stable patients to reduce cardiovascular mortality when used in conjunction with oral metoprolol maintenance therapy. Metoprolol Tartrate Injection is a beta-adrenergic receptor inhibitor indicated for the treatment of definite or suspected acute myocardial infarction in hemodynamically stable patients to reduce cardiovascular mortality when used in conjunction with oral metoprolol maintenance therapy ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0143-9873

What is NDC 0143-9873?: 0143-9873 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 5 mg/5mL injection, solution, listed with the FDA by Hikma Pharmaceuticals USA Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Metoprolol Tartrate.
What is the active ingredient?: Metoprolol tartrate.
Who is the labeler?: Hikma Pharmaceuticals USA Inc., NDC labeler code 0143. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Metoprolol Tartrate?: 224 other product NDCs are listed under this name. See all Metoprolol Tartrate 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 Metoprolol Tartrate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Metoprolol Tartratemetoprolol	Metoprolol tartrate 50 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-944	60760-0944-60
Metoprolol Tartrate	Metoprolol tartrate 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-4748	70518-4748-00
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-4714	70518-4714-00
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0278	55154-0278-00
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0279	55154-0279-00
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	TabletOral	Direct_Rx	72189-677	72189-0677-90
Metoprolol Tartratemetoprolol	Metoprolol tartrate 100 mg/1	TabletOral	Coupler LLC	67046-1384	67046-1384-03
Metoprolol Tartrate	Metoprolol tartrate 100 mg/1	TabletOral	ST. MARY'S MEDICAL PARK PHARMACY	60760-928	60760-0928-90
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-555	72789-0555-90
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	Tablet, Film coatedOral	Safecor Health, LLC	48433-073	48433-0073-20

All 225 Metoprolol Tartrate NDCs

Other NDCs under ANDA 077761

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

FDA NDC Directory listings under ANDA 077761
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol Tartratemetoroprolol tartrate	Metoprolol tartrate 5 mg/5mL	Injection, SolutionIntravenous	Hikma Pharmaceuticals USA Inc.	0143-9660
Metoprolol Tartrate	Metoprolol tartrate 5 mg/5mL	Injection, SolutionIntravenous	Medical Purchasing Solutions, LLC	71872-7225
Metoprolol Tartratemetoroprolol tartrate	Metoprolol tartrate 5 mg/5mL	Injection, SolutionIntravenous	Medical Purchasing Solutions, LLC	71872-7244
Metoprolol Tartratemetoroprolol tartrate	Metoprolol tartrate 5 mg/5mL	Injection, SolutionIntravenous	Civica, Inc.	72572-420