What is NDC 68071-3432?

68071-3432 is the product NDC for Venlafaxine, Venlafaxine hydrochloride 75 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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?

116 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 68071-3432 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-3432Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-3432Add 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
68071-3432-0	68071343200	100 TABLET in 1 BOTTLE (68071-3432-0)Marketed from Jun 19, 2023

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): Venlafaxine
Generic name (nonproprietary): venlafaxine
Active ingredients: Venlafaxine hydrochloride — 75 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077653
Marketing start: Jun 13, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 68071-3432_2d5887b5-8622-42a8-e063-6394a90a1b2eSPL ID 2d5887b5-8622-42a8-e063-6394a90a1b2eSPL set ID fe7de51e-8a81-fe68-e053-6294a90a7339RxCUI 313586UNII 7D7RX5A8MOUPC 0368071343205
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

N468071343200 followed by a unit qualifier and the quantity

Package 68071-3432-00. 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 4, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Venlafaxine tablets, USP are 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 incl…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-3432

What is NDC 68071-3432?: 68071-3432 is the product NDC for Venlafaxine, Venlafaxine hydrochloride 75 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, 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?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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?: 116 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)
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
Venlafaxine	Venlafaxine hydrochloride 225 mg/1	Tablet, Extended releaseOral	Ajanta Pharma USA Inc.	27241-224	27241-0224-3027241-0224-90

All 117 Venlafaxine NDCs

Other NDCs under ANDA 077653

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

FDA NDC Directory listings under ANDA 077653
Product	Strength	Form · route	Labeler	Product NDC
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	A-S Medication Solutions	50090-2408
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	A-S Medication Solutions	50090-4865
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-728
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	Proficient Rx LP	63187-414
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	Bryant Ranch Prepack	63629-3324
Venlafaxine	Venlafaxine hydrochloride 100 mg/1	TabletOral	BluePoint Laboratories	68001-156
Venlafaxine	Venlafaxine hydrochloride 25 mg/1	TabletOral	BluePoint Laboratories	68001-157
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	BluePoint Laboratories	68001-158
Venlafaxine	Venlafaxine hydrochloride 50 mg/1	TabletOral	BluePoint Laboratories	68001-159
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	BluePoint Laboratories	68001-160
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-2990
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3431
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	American Health Packaging	68084-844
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	American Health Packaging	68084-856
Venlafaxine	Venlafaxine hydrochloride 25 mg/1	TabletOral	American Health Packaging	68084-896
Venlafaxine	Venlafaxine hydrochloride 25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-018
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-019
Venlafaxine	Venlafaxine hydrochloride 50 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-020
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-021
Venlafaxine	Venlafaxine hydrochloride 100 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-101

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