What is NDC 71335-0149?

71335-0149 is the product NDC for Metoprolol succinate, Metoprolol succinate 50 mg/1 tablet, extended release, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, shown above in 10- and 11-digit form.

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 succinate?

250 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Metoprolol succinate NDC 71335-0149

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0149Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0149Add 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
71335-0149-1	7133501490171335014901	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-1)Marketed from Jan 28, 2014
71335-0149-2	7133501490271335014902	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-2)Marketed from Jan 28, 2014
71335-0149-3	7133501490371335014903	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-3)Marketed from Jan 28, 2014
71335-0149-4	7133501490471335014904	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-4)Marketed from Jan 28, 2014
71335-0149-5	7133501490571335014905	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-5)Marketed from Jan 28, 2014

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 succinate
Generic name (nonproprietary): metoprolol succinate
Active ingredients: Metoprolol succinate — 50 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090617
Marketing start: Sep 10, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 71335-0149_609cf08a-a8d7-4e20-83e6-05823fb89286SPL ID 609cf08a-a8d7-4e20-83e6-05823fb89286SPL set ID 42bb324d-8b1e-45db-b15e-3845eec83c38RxCUI 866427, 866436UNII TH25PD4CCB
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

N471335014901 followed by a unit qualifier and the quantity

Package 71335-0149-01. 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 Dec 5, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

Metoprolol succinate extended-release tablets, metoprolol succinate, is a beta 1 -selective adrenoceptor blocking agent. Metoprolol succinate extended-release tablets are 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 ) Heart Failure - for the treatment of stable, symptomatic (NYHA Class II or III) heart failure of ischemic, hypertensive, or cardiomyopathic origin.( 1.3) 1.1 Hypertension Metoprolol succinate extended-release tablets are indicated for the treatment of hypertension, to lower blood pressure. Lo…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0149

What is NDC 71335-0149?: 71335-0149 is the product NDC for Metoprolol succinate, Metoprolol succinate 50 mg/1 tablet, extended release, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Metoprolol succinate.
What is the active ingredient?: Metoprolol succinate.
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 succinate?: 250 other product NDCs are listed under this name. See all Metoprolol succinate 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 succinate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-0883	67046-0883-03
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1685	67046-1685-03
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1686	67046-1686-03
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Oryza pharmaceuticals Inc.	72516-025	72516-0025-0172516-0025-1072516-0025-50
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-684	68001-0684-0068001-0684-03
Metoprolol Succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-685	68001-0685-0068001-0685-03
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-686	68001-0686-0068001-0686-03
Metoprolol Succinate	Metoprolol succinate 200 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-687	68001-0687-00
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1650	67046-1650-03
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	53401-009	53401-0009-3053401-0009-4553401-0009-53+3 more

All 251 Metoprolol succinate NDCs

Other NDCs under ANDA 090617

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

FDA NDC Directory listings under ANDA 090617
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	53401-010
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	53401-009
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceutcals, Inc.	68071-3828
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Cardinal Health 107, LLC	55154-7280
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-0158
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Cardinal Health 107, LLC	55154-2642
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Northstar Rx LLC	72603-142
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Northstar Rx LLC	72603-143
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7118
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7117
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	AvPAK	50268-540
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-7823
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	AvPAK	50268-541
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	43063-624
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-7824
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Dr. Reddy's Laboratories Inc	75907-347
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Dr. Reddy's Laboratories Inc	75907-344
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6322
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6323
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Quallent Pharmaceuticals Health LLC	82009-113

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