Metoprolol Tartrate NDC 55289-382

Product information

Brand name (proprietary)

Metoprolol Tartrate

Generic name (nonproprietary)

metoprolol tartrate

Active ingredients

Metoprolol tartrate — 25 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

PD-Rx Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 076704

Marketing start

Feb 23, 2004

Listing expires

Dec 31, 2027

Other FDA classes

Adrenergic beta-Antagonists (Mechanism)

Identifiers

Product ID 55289-382_525a6d19-36b4-ca74-e063-6294a90a03cbSPL ID 525a6d19-36b4-ca74-e063-6294a90a03cbSPL set ID ab44f4c5-9497-4c92-8545-e4718ddb8f08RxCUI 866924UNII W5S57Y3A5LUPC 0355289382904

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

N455289038214 followed by a unit qualifier and the quantity Copy

Package 55289-0382-14. 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

Other NDCs under ANDA 076704

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