Prescription drug · ANDA

Metoprolol Tartrate NDC 52817-358

Metoprolol tartrate 37.5 mg/1 · Tablet, Film coated · Oral · TruPharma LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)52817-358Labeler and product segments. Claims need a package NDC.
Product NDC at billing width52817-0358Add 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 NDC11-digit (billing)PackageCopy
52817-358-1052817035810100 TABLET, FILM COATED in 1 PACKAGE (52817-358-10)Marketed from Dec 1, 2018 · Sample package
52817-358-5052817035850500 TABLET, FILM COATED in 1 PACKAGE (52817-358-50)Marketed from Dec 1, 2018

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 — 37.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200981
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 52817-358_294dc99d-4a6d-22b6-e063-6394a90a06aaSPL ID 294dc99d-4a6d-22b6-e063-6394a90a06aaSPL set ID 52c822f2-4a71-4ab2-a470-58074622846aRxCUI 866511, 866514, 866924, 1606347, 1606349UNII W5S57Y3A5LUPC 0352817361103, 0352817361004, 0352817360106, 0352817362100, 0352817358509, 0352817359506, 0352817362001, 0352817360007, 0352817358103, 0352817359100
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

N452817035810 followed by a unit qualifier and the quantity

Package 52817-0358-10. 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 .

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)

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
ProductStrengthForm · routeLabelerProduct NDC
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-555
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-680
Metoprolol TartrateMetoprolol tartrate 100 mg/1TabletOralDirect_Rx72189-659
Metoprolol TartrateMetoprolol tartrate 25 mg/1TabletOralREMEDYREPACK INC.70518-4714
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3793
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8509
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralAdvagen Pharma Limited72888-004
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralQPharma, Inc.42708-198
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralBryant Ranch Prepack71335-2656
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralDirect_Rx72189-677
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralAdvagen Pharma Limited72888-005
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralAdvagen Pharma Limited72888-006
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6764
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6763
Metoprolol TartrateMetoprolol tartrate 75 mg/1Tablet, Film coatedOralAdvagen Pharma Limited72888-023
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralProficient Rx LP82804-165
Metoprolol TartrateMetoprolol tartrate 100 mg/1TabletOralBryant Ranch Prepack71335-2675
Metoprolol TartrateMetoprolol tartrate 100 mg/1TabletOralREMEDYREPACK INC.70518-4748
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralA-S Medication Solutions50090-7969
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralA-S Medication Solutions50090-7970

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Metoprolol Tartrate NDC 52817-358 | Med-Code