What is NDC 71335-1331?

71335-1331 is the product NDC for Desvenlafaxine Succinate, Desvenlafaxine succinate 100 mg/1 tablet, film coated, extended release, listed with the FDA by Bryant Ranch Prepack. It has 4 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 Succinate?

10 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Desvenlafaxine Succinate NDC 71335-1331

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-1331Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-1331Add 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
71335-1331-1	7133513310171335133101	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1331-1)Marketed from Sep 3, 2019
71335-1331-2	7133513310271335133102	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1331-2)Marketed from May 20, 2024
71335-1331-3	7133513310371335133103	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1331-3)Marketed from May 20, 2024
71335-1331-4	7133513310471335133104	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1331-4)Marketed from May 20, 2024

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 Succinate
Generic name (nonproprietary): desvenlafaxine succinate
Active ingredients: Desvenlafaxine succinate — 100 mg/1
Dosage form: Tablet, Film coated, 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 204172
Marketing start: Mar 1, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 2D6 Inhibitors (Mechanism)Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 71335-1331_20d898df-2d0e-462b-a10e-99b51f5c1522SPL ID 20d898df-2d0e-462b-a10e-99b51f5c1522SPL set ID 56c9e8ee-1460-4a4c-8033-65d9afb358c8RxCUI 1874553UNII 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

N471335133101 followed by a unit qualifier and the quantity

Package 71335-1331-01. 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 Jun 12, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Desvenlafaxine extended-release tablet is indicated for the treatment of adults with major depressive disorder (MDD) [see CLINICAL STUDIES ( 14 )]. Desvenlafaxine extended-release tablet, is 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 71335-1331

What is NDC 71335-1331?: 71335-1331 is the product NDC for Desvenlafaxine Succinate, Desvenlafaxine succinate 100 mg/1 tablet, film coated, extended release, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Desvenlafaxine Succinate.
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 Succinate?: 10 other product NDCs are listed under this name. See all Desvenlafaxine 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 Desvenlafaxine Succinate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8556	68788-8556-0168788-8556-0368788-8556-06+1 more
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-7468	50090-7468-0050090-7468-01
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-604	68180-0604-06
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-2494	71335-2494-0171335-2494-0271335-2494-03+1 more
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Macleods Pharmaceuticals Limited	33342-388	33342-0388-0733342-0388-1033342-0388-12
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	Macleods Pharmaceuticals Limited	33342-389	33342-0389-0733342-0389-1033342-0389-12
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-6894	50090-6894-00
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-592	68180-0592-06
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-593	68180-0593-06
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-1150	71335-1150-0171335-1150-0271335-1150-03+2 more

Other NDCs under ANDA 204172

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

FDA NDC Directory listings under ANDA 204172
Product	Strength	Form · route	Labeler	Product NDC
Desvenlafaxine ER	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Direct_Rx	61919-882
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-6894
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-7468
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-592
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-593
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-604
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8556
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-1150
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-2494