What is NDC 71335-2575?

71335-2575 is the product NDC for Desvenlafaxine, Desvenlafaxine 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 Desvenlafaxine?

52 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Desvenlafaxine NDC 71335-2575 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2575Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2575Add 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
71335-2575-1	7133525750171335257501	30 TABLET, EXTENDED RELEASE in 1 PACKAGE (71335-2575-1)Marketed from Feb 5, 2025
71335-2575-2	7133525750271335257502	28 TABLET, EXTENDED RELEASE in 1 PACKAGE (71335-2575-2)Marketed from Feb 5, 2025
71335-2575-3	7133525750371335257503	60 TABLET, EXTENDED RELEASE in 1 PACKAGE (71335-2575-3)Marketed from Feb 5, 2025
71335-2575-4	7133525750471335257504	90 TABLET, EXTENDED RELEASE in 1 PACKAGE (71335-2575-4)Marketed from Feb 5, 2025
71335-2575-5	7133525750571335257505	180 TABLET, EXTENDED RELEASE in 1 PACKAGE (71335-2575-5)Marketed from Feb 5, 2025

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): Desvenlafaxine
Generic name (nonproprietary): desvenlafaxine
Active ingredients: Desvenlafaxine 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 204028
Marketing start: Jan 31, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 2D6 Inhibitors (Mechanism)Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 71335-2575_c69838a2-6378-4bb4-9109-607fe77550cbSPL ID c69838a2-6378-4bb4-9109-607fe77550cbSPL set ID 5b6e86bc-24a3-4f8c-aff7-6e1e17a7d1a4RxCUI 1874559UNII ZB22ENF0XR
Pharmacologic class: Serotonin and Norepinephrine Reuptake Inhibitor

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

N471335257501 followed by a unit qualifier and the quantity

Package 71335-2575-01. 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 Feb 5, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Desvenlafaxine extended-release tablets are indicated for the treatment of adults with major depressive disorder (MDD) [see Clinical Studies (14) ]. Desvenlafaxine Extended-Release Tablets are a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of adults with major depressive disorder (MDD) ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2575

What is NDC 71335-2575?: 71335-2575 is the product NDC for Desvenlafaxine, Desvenlafaxine 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?: Desvenlafaxine.
What is the active ingredient?: Desvenlafaxine 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 Desvenlafaxine?: 52 other product NDCs are listed under this name. See all Desvenlafaxine 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 Desvenlafaxine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Marlex Pharmaceuticals, Inc.	10135-821	10135-0821-1010135-0821-1410135-0821-30+1 more
Desvenlafaxine	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	Marlex Pharmaceuticals, Inc.	10135-822	10135-0822-1010135-0822-1410135-0822-30+1 more
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals, Inc.	68071-5332	68071-5332-03
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-555	72603-0555-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-556	72603-0556-0172603-0556-02
Desvenlafaxine	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-557	72603-0557-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8760	68788-8760-0168788-8760-0368788-8760-06+1 more
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7190	50090-7190-0050090-7190-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7737	50090-7737-0050090-7737-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-3790	68071-3790-03

All 53 Desvenlafaxine NDCs

Other NDCs under ANDA 204028

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

FDA NDC Directory listings under ANDA 204028
Product	Strength	Form · route	Labeler	Product NDC
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8760
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-555
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-556
Desvenlafaxine	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-557
Desvenlafaxine ER	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Direct_rx	72189-567
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Advagen Pharma Ltd	72888-143
Desvenlafaxine	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	Advagen Pharma Ltd	72888-144
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7190
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7737
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	Advagen Pharma Ltd	72888-175
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals, Inc.	68071-5332
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-3790
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-2490
Desvenlafaxine	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-2512