What is NDC 47335-794?

47335-794 is the product NDC for Venlafaxine Hydrochloride, Venlafaxine hydrochloride 225 mg/1 tablet, extended release, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 6 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 47335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Venlafaxine Hydrochloride?

208 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Venlafaxine Hydrochloride NDC 47335-794

NDC codes

FDA NDC Directory

Product NDC (as listed)47335-794Labeler and product segments. Claims need a package NDC.

Product NDC at billing width47335-0794Add 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
47335-794-08	47335079408	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08)Marketed from Feb 15, 2019
47335-794-13	47335079413	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13)Marketed from Feb 15, 2019
47335-794-81	47335079481	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81)Marketed from Aug 15, 2019
47335-794-83	47335079483	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-83)Marketed from Feb 15, 2019
47335-794-88	47335079488	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-88)Marketed from Feb 15, 2019
47335-794-99	47335079499	5 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-794-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Feb 15, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Venlafaxine Hydrochloride
Generic name (nonproprietary): venlafaxine hydrochloride
Active ingredients: Venlafaxine hydrochloride — 225 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 47335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091272
Marketing start: Feb 15, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 47335-794_dae15132-d26b-4ea9-b937-da9c282ada48SPL ID dae15132-d26b-4ea9-b937-da9c282ada48SPL set ID dc989aa7-c4ab-4359-a971-523eb477ef9bRxCUI 808744, 808748, 808751, 808753UNII 7D7RX5A8MOUPC 0347335794830
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

N447335079408 followed by a unit qualifier and the quantity

Package 47335-0794-08. 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 Sep 15, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

Venlafaxine hydrochloride extended-release tablets are a selective serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for: Major Depressive Disorder (MDD) ( 1.1 ) Social Anxiety Disorder (SAD) ( 1.2 ) 1.1 Major Depressive Disorder Venlafaxine hydrochloride extended-release tablets are indicated for the treatment of major depressive disorder (MDD). Efficacy of venlafaxine in MDD was shown in both short-term trials and a longer-term trial in MDD [ see Clinical Studies ( 14.1 ) ]. A major depressive episode (DSM-IV) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed mood or the loss of interest or pleasure in nearly all activities, repr…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 47335-794

What is NDC 47335-794?: 47335-794 is the product NDC for Venlafaxine Hydrochloride, Venlafaxine hydrochloride 225 mg/1 tablet, extended release, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Venlafaxine Hydrochloride.
What is the active ingredient?: Venlafaxine hydrochloride.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 47335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Venlafaxine Hydrochloride?: 208 other product NDCs are listed under this name. See all Venlafaxine Hydrochloride 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 Venlafaxine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	24658-125	24658-0125-1024658-0125-3024658-0125-90
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	24658-126	24658-0126-1024658-0126-3024658-0126-90
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	24658-127	24658-0127-0524658-0127-3024658-0127-90
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	Coupler LLC	67046-0390	67046-0390-03
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	Coupler LLC	67046-0527	67046-0527-03
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	NorthStar RxLLC	72603-747	72603-0747-01
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	NorthStar RxLLC	72603-748	72603-0748-01
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	NorthStar RxLLC	72603-749	72603-0749-01
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	REMEDYREPACK INC.	70518-4632	70518-4632-00
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	Advanced Rx of Tennessee, LLC	80425-0581	80425-0581-0180425-0581-0280425-0581-03

All 209 Venlafaxine Hydrochloride NDCs

Other NDCs under ANDA 091272

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

FDA NDC Directory listings under ANDA 091272
Product	Strength	Form · route	Labeler	Product NDC
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 150 mg/1	Tablet, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-758
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 75 mg/1	Tablet, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-759
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Tablet, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-760