What is NDC 68071-4880?

68071-4880 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 100 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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?

223 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 68071-4880 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-4880Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-4880Add 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
68071-4880-1	68071488001	120 TABLET, FILM COATED in 1 BOTTLE (68071-4880-1)Marketed from May 2, 2019
68071-4880-9	68071488009	90 TABLET, FILM COATED in 1 BOTTLE (68071-4880-9)Marketed from May 2, 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): Metoprolol Tartrate
Generic name (nonproprietary): metoprolol tartrate
Active ingredients: Metoprolol tartrate — 100 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200981
Marketing start: Dec 1, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 68071-4880_1ae1cc9d-0254-361f-e063-6394a90a966bSPL ID 1ae1cc9d-0254-361f-e063-6394a90a966bSPL set ID 87ef9aa6-2faa-0f77-e053-2a95a90a3a26RxCUI 866511UNII W5S57Y3A5LUPC 0368071488098
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 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

N468071488001 followed by a unit qualifier and the quantity

Package 68071-4880-01. 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 Jun 14, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Metoprolol tartrate tablets are indicated for the treatment of hypertension. They may be used alone or in combination with other antihypertensive agents. Angina Pectoris Metoprolol tartrate tablets are indicated in the long-term treatment of angina pectoris. Myocardial Infarction Metoprolol tartrate tablets are indicated in the treatment of hemodynamically stable patients with definite or suspected acute myocardial infarction to reduce cardiovascular mortality when used alone or in conjunction with intravenous metoprolol. Oral Metoprolol tartrate tablets therapy can be initiated after intravenous metoprolol therapy or, alternatively, oral treatment can begi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-4880

What is NDC 68071-4880?: 68071-4880 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 100 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,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?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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?: 223 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 224 Metoprolol Tartrate NDCs

Other NDCs under ANDA 200981

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

FDA NDC Directory listings under ANDA 200981
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	TabletOral	A-S Medication Solutions	50090-7738
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8886
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	TabletOral	Proficient Rx LP	82804-253
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2164
Metoprolol Tartrate	Metoprolol tartrate 100 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3935
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8211
Metoprolol Tartrate	Metoprolol tartrate 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-4535
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-5236
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-4308
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-3950
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3946
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-4755
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	TabletOral	TRUPHARMA LLC	52817-250
Metoprolol Tartrate	Metoprolol tartrate 25 mg/1	TabletOral	Coupler LLC	67046-1561
Metoprolol Tartrate	Metoprolol tartrate 75 mg/1	TabletOral	TRUPHARMA LLC	52817-253
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6083
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6084
Metoprolol Tartrate	Metoprolol tartrate 37.5 mg/1	TabletOral	TRUPHARMA LLC	52817-251
Metoprolol Tartrate	Metoprolol tartrate 50 mg/1	TabletOral	TRUPHARMA LLC	52817-252
Metoprolol Tartrate	Metoprolol tartrate 100 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8249

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