What is NDC 51662-1478?

51662-1478 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 1 mg/mL injection, solution, listed with the FDA by HF Acquisition Co LLC, DBA HealthFirst. It has 1 package NDC, shown above in 10- and 11-digit form.

HF Acquisition Co LLC, DBA HealthFirst, NDC labeler code 51662. 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 51662-1478

NDC codes

FDA NDC Directory

Product NDC (as listed)51662-1478Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51662-1478Add 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
51662-1478-3	5166214780351662147803	10 POUCH in 1 CASE (51662-1478-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1478-2) / 5 mL in 1 VIAL, SINGLE-DOSE (51662-1478-1)Marketed from Sep 24, 2023

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): Metoprolol Tartrate
Generic name (nonproprietary): metoprolol tartrate
Active ingredients: Metoprolol tartrate — 1 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: HF Acquisition Co LLC, DBA HealthFirstNDC labeler code 51662
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078085
Marketing start: Dec 14, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 51662-1478_12009af9-def3-b2ad-e063-6294a90af85dSPL ID 12009af9-def3-b2ad-e063-6294a90af85dSPL set ID 99b22be0-d2b4-2449-e053-2995a90a6c28RxCUI 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

N451662147803 followed by a unit qualifier and the quantity

Package 51662-1478-03. 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 22, 2024.

Indications (excerpt from the label)

INDICATIONS & USAGE Myocardial Infarction Metoprolol tartrate injection is indicated in the treatment of hemodynamically stable patients with definite or suspected acute myocardial infarction to reduce cardiovascular mortality when used in conjunction with oral metoprolol tartrate maintenance therapy. Treatment with intravenous metoprolol tartrate can be initiated as soon as the patient's clinical condition allows (see DOSAGE AND ADMINISTRATION, CONTRAINDICATIONS , and WARNINGS ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51662-1478

What is NDC 51662-1478?: 51662-1478 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 1 mg/mL injection, solution, listed with the FDA by HF Acquisition Co LLC, DBA HealthFirst. It has 1 package NDC, 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?: HF Acquisition Co LLC, DBA HealthFirst, NDC labeler code 51662. 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 078085

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

FDA NDC Directory listings under ANDA 078085
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol Tartrate	Metoprolol tartrate 1 mg/mL	Injection, SolutionIntravenous	Hospira, Inc.	0409-1778
Metoprolol Tartrate	Metoprolol tartrate 1 mg/mL	Injection, SolutionIntravenous	Hospira, Inc.	0409-2016
Metoprolol Tartrate	Metoprolol tartrate 1 mg/mL	Injection, SolutionIntravenous	Cardinal Health 107, LLC	55154-4745
Metoprolol Tartrate	Metoprolol tartrate 1 mg/mL	Injection, SolutionIntravenous	ProPharma Distribution	84549-778