NDC codes

FDA NDC Directory
Product NDC (as listed)50090-1979Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-1979Add 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
50090-1979-05009019790030 TABLET, FILM COATED in 1 BOTTLE (50090-1979-0)Marketed from Jul 1, 2019
50090-1979-15009019790160 TABLET, FILM COATED in 1 BOTTLE (50090-1979-1)Marketed from Sep 10, 2015
50090-1979-45009019790490 TABLET, FILM COATED in 1 BOTTLE (50090-1979-4)Marketed from Sep 10, 2015
50090-1979-550090197905180 TABLET, FILM COATED in 1 BOTTLE (50090-1979-5)Marketed from Sep 10, 2015

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 tartrate50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077739
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 50090-1979_213d34c0-3a02-4408-8ed7-d3d91e8ed9c3SPL ID 213d34c0-3a02-4408-8ed7-d3d91e8ed9c3SPL set ID e1bb16fa-4f72-44bc-bc33-d7653c13f55cRxCUI 866511, 866514UNII 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 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

N450090197900 followed by a unit qualifier and the quantity

Package 50090-1979-00. 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 .

Indications (excerpt from the label)

Metoprolol tartrate tablets are 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 are indicated for the treatment of hypertension in adult patients, to lower blood pressure. Lowering blood pressure lo

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077739

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

FDA NDC Directory listings under ANDA 077739
ProductStrengthForm · routeLabelerProduct NDC
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-534
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-821
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-535
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7362
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7363
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-514
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-953
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-954
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-549
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-527
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralLegacy Pharmaceutical Packaging, LLC68645-191
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-080
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralLegacy Pharmaceutical Packaging, LLC68645-190
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1974
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-927
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-938
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-138
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-137
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-147
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3291

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