What is NDC 23155-246?

23155-246 is the product NDC for Venlafaxine, Venlafaxine hydrochloride 25 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. 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?

118 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Venlafaxine NDC 23155-246 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)23155-246Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23155-0246Add 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	Copy
23155-246-01	2315502460123155024601	100 TABLET in 1 BOTTLE (23155-246-01)Marketed from Jul 19, 2021
23155-246-09	2315502460923155024609	90 TABLET in 1 BOTTLE (23155-246-09)Marketed from Jul 19, 2021

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
Generic name (nonproprietary): venlafaxine
Active ingredients: Venlafaxine hydrochloride — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.NDC labeler code 23155
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078554
Marketing start: Jul 19, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 23155-246_da564fb4-3f43-4725-b5f2-e5826bfc2170SPL ID da564fb4-3f43-4725-b5f2-e5826bfc2170SPL set ID 80ac757d-c629-4579-8afd-cae0ee9cd614RxCUI 313580, 313582, 313584, 313586, 314277UNII 7D7RX5A8MO
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

N423155024601 followed by a unit qualifier and the quantity

Package 23155-0246-01. 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 19, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Venlafaxine tablets, USP is indicated for the treatment of major depressive disorder. The efficacy of Venlafaxine tablets USP in the treatment of major depressive disorder was established in 6 week controlled trials of adult outpatients whose diagnoses corresponded most closely to the DSM-III or DSM-III-R category of major depression and in a 4 week controlled trial of inpatients meeting diagnostic criteria for major depression with melancholia (see CLINICAL TRIALS ). A major depressive episode implies a prominent and relatively persistent depressed or dysphoric mood that usually interferes with daily functioning (nearly every day for at least 2 weeks); it should includ…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-246

What is NDC 23155-246?: 23155-246 is the product NDC for Venlafaxine, Venlafaxine hydrochloride 25 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Venlafaxine.
What is the active ingredient?: Venlafaxine hydrochloride.
Who is the labeler?: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. 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?: 118 other product NDCs are listed under this name. See all Venlafaxine 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4779	70518-4779-00
venlafaxinevenlafaxine hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	Coupler LLC	67046-0560	67046-0560-03
venlafaxine	Venlafaxine hydrochloride 50 mg/1	TabletOral	Coupler LLC	67046-1681	67046-1681-03
venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	Coupler LLC	67046-2020	67046-2020-03
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4566	70518-4566-00
Venlafaxine	Venlafaxine hydrochloride 150 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4500	70518-4500-00
venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	REMEDYREPACK INC.	70518-4168	70518-4168-00
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-3820	70518-3820-00
venlafaxinevenlafaxine hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	Northwind Health Company, LLC	51655-323	51655-0323-52
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-728	60760-0728-60

All 119 Venlafaxine NDCs

Other NDCs under ANDA 078554

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

FDA NDC Directory listings under ANDA 078554
Product	Strength	Form · route	Labeler	Product NDC
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-247
Venlafaxine	Venlafaxine hydrochloride 50 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-248
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-249
Venlafaxine	Venlafaxine hydrochloride 100 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-250