NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1600Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1600Add 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
71335-1600-17133516000130 TABLET, FILM COATED in 1 BOTTLE (71335-1600-1)Marketed from Jun 12, 2020
71335-1600-27133516000260 TABLET, FILM COATED in 1 BOTTLE (71335-1600-2)Marketed from Feb 14, 2022
71335-1600-37133516000390 TABLET, FILM COATED in 1 BOTTLE (71335-1600-3)Marketed from Feb 14, 2022
71335-1600-471335160004180 TABLET, FILM COATED in 1 BOTTLE (71335-1600-4)Marketed from Feb 14, 2022
71335-1600-571335160005100 TABLET, FILM COATED in 1 BOTTLE (71335-1600-5)Marketed from Feb 14, 2022
71335-1600-671335160006120 TABLET, FILM COATED in 1 BOTTLE (71335-1600-6)Marketed from Feb 14, 2022
71335-1600-77133516000720 TABLET, FILM COATED in 1 BOTTLE (71335-1600-7)Marketed from Feb 14, 2022
71335-1600-87133516000810 TABLET, FILM COATED in 1 BOTTLE (71335-1600-8)Marketed from Feb 14, 2022

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 — 25 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
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 71335-1600_da8cd7af-031c-4abc-84d4-71686cf113d2SPL ID da8cd7af-031c-4abc-84d4-71686cf113d2SPL set ID a590edb1-3310-49e3-b3d1-dbbb3f81f1c1RxCUI 866924UNII 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

N471335160001 followed by a unit qualifier and the quantity

Package 71335-1600-01. 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 .

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 71335-1600

What is NDC 71335-1600?
71335-1600 is the product NDC for Metoprolol Tartrate, Metoprolol tartrate 25 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 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?
Bryant Ranch Prepack, NDC labeler code 71335. 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?
221 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Metoprolol TartratemetoprololMetoprolol tartrate 50 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-94460760-0944-60
Metoprolol TartrateMetoprolol tartrate 100 mg/1TabletOralREMEDYREPACK INC.70518-474870518-4748-00
Metoprolol TartrateMetoprolol tartrate 25 mg/1TabletOralREMEDYREPACK INC.70518-471470518-4714-00
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-027855154-0278-00
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-027955154-0279-00
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralDirect_Rx72189-67772189-0677-90
Metoprolol TartratemetoprololMetoprolol tartrate 100 mg/1TabletOralCoupler LLC67046-138467046-1384-03
Metoprolol TartrateMetoprolol tartrate 100 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-92860760-0928-90
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-55572789-0555-90
Metoprolol TartrateMetoprolol tartrate 25 mg/1Tablet, Film coatedOralSafecor Health, LLC48433-07348433-0073-20

All 222 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
ProductStrengthForm · routeLabelerProduct NDC
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralQPharma, Inc.42708-198
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6083
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6084
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6763
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6764
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralA-S Medication Solutions50090-7553
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralA-S Medication Solutions50090-7554
Metoprolol TartrateMetoprolol tartrate 25 mg/1TabletOralA-S Medication Solutions50090-7567
Metoprolol TartrateMetoprolol tartrate 25 mg/1TabletOralA-S Medication Solutions50090-7568
Metoprolol TartrateMetoprolol tartrate 100 mg/1TabletOralA-S Medication Solutions50090-7569
Metoprolol TartrateMetoprolol tartrate 100 mg/1TabletOralA-S Medication Solutions50090-7570
Metoprolol TartrateMetoprolol tartrate 25 mg/1TabletOralA-S Medication Solutions50090-7738
Metoprolol TartrateMetoprolol tartrate 25 mg/1TabletOralA-S Medication Solutions50090-7739
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7740
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7741
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralA-S Medication Solutions50090-7969
Metoprolol TartrateMetoprolol tartrate 50 mg/1TabletOralA-S Medication Solutions50090-7970
Metoprolol TartrateMetoprolol tartrate 50 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-281
Metoprolol TartrateMetoprolol tartrate 100 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-884
Metoprolol TartrateMetoprolol tartrate 25 mg/1TabletOralTRUPHARMA LLC52817-250

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