What is NDC 82804-978?

82804-978 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 50 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 6 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 82804. 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 82804-978 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)82804-978Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82804-0978Add 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
82804-978-00	8280409780082804097800	100 TABLET in 1 BOTTLE (82804-978-00)Marketed from Mar 11, 2025
82804-978-11	8280409781182804097811	1000 TABLET in 1 BOTTLE (82804-978-11)Marketed from Mar 11, 2025
82804-978-30	8280409783082804097830	30 TABLET in 1 BOTTLE (82804-978-30)Marketed from Mar 11, 2025
82804-978-55	8280409785582804097855	500 TABLET in 1 BOTTLE (82804-978-55)Marketed from Mar 11, 2025
82804-978-60	8280409786082804097860	60 TABLET in 1 BOTTLE (82804-978-60)Marketed from Mar 11, 2025
82804-978-90	8280409789082804097890	90 TABLET in 1 BOTTLE (82804-978-90)Marketed from Mar 11, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 82804
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074453
Marketing start: Nov 2, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 82804-978_de781298-37cb-4c03-8431-b6d86ffbde0dSPL ID de781298-37cb-4c03-8431-b6d86ffbde0dSPL set ID de781298-37cb-4c03-8431-b6d86ffbde0dRxCUI 866511, 866514UNII W5S57Y3A5LUPC 0382804979301, 0382804978304
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

N482804097800 followed by a unit qualifier and the quantity

Package 82804-0978-00. 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 Mar 1, 2025.

Indications (excerpt from the label)

1. INDICATIONS AND USAGE Metoprolol tartrate tablets is a beta-adrenergic blocker indicated for the treatment of: • Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) • Angina Pectoris. ( 1.2 ) • Myocardial Infarction, to reduce the risk of cardiovascular mortality when used in conjunction with intravenous metoprolol therapy in patients with definite or suspected acute myocardial infarction in hemodynamically stable patients. ( 1.3 ) 1.1 Hypertension Metoprolol tartrate tablets, USP is indicated for the treatment of hypertension in adult patients, to lower blood pr…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82804-978

What is NDC 82804-978?: 82804-978 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 50 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 6 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?: Proficient Rx LP, NDC labeler code 82804. 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 074453

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

FDA NDC Directory listings under ANDA 074453
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol Tartrate	Metoprolol tartrate 100 mg/1	TabletOral	Proficient Rx LP	82804-979