What is NDC 65841-751?

65841-751 is the product NDC for venlafaxine hydrochloride, Venlafaxine hydrochloride 37.5 mg/1 capsule, extended release, listed with the FDA by Zydus Lifesciences Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 65841. 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?

207 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 65841-751

NDC codes

FDA NDC Directory

Product NDC (as listed)65841-751Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65841-0751Add 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
65841-751-06	6584107510665841075106	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-06)Marketed from Jun 1, 2011
65841-751-10	6584107511065841075110	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-10)Marketed from Jun 1, 2011
65841-751-16	6584107511665841075116	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-16)Marketed from Jun 1, 2011

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 — 37.5 mg/1
Dosage form: Capsule, Extended release
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 65841
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090174
Marketing start: Jun 1, 2011
Listing expires: Dec 31, 2027
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 65841-751_f20749dc-d1f6-4860-b583-82b82d3a2242SPL ID f20749dc-d1f6-4860-b583-82b82d3a2242SPL set ID 1be1be3a-304b-4e31-8732-335247029191RxCUI 313581, 313583, 313585UNII 7D7RX5A8MOUPC 0365841752106, 0365841753103
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

N465841075106 followed by a unit qualifier and the quantity

Package 65841-0751-06. 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 28, 2023.

Full label on DailyMed (opens in a new tab)

About NDC 65841-751

What is NDC 65841-751?: 65841-751 is the product NDC for venlafaxine hydrochloride, Venlafaxine hydrochloride 37.5 mg/1 capsule, extended release, listed with the FDA by Zydus Lifesciences Limited. It has 3 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?: Zydus Lifesciences Limited, NDC labeler code 65841. 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?: 207 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 208 venlafaxine hydrochloride NDCs

Other NDCs under ANDA 090174

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

FDA NDC Directory listings under ANDA 090174
Product	Strength	Form · route	Labeler	Product NDC
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8774
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	Zydus Pharmaceuticals USA Inc.	70710-1700
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	Zydus Pharmaceuticals USA Inc.	70710-1698
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	Zydus Pharmaceuticals USA Inc.	70710-1699
venlafaxine hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-4442
venlafaxine hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	Zydus Lifesciences Limited	65841-753
venlafaxine hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	Zydus Lifesciences Limited	65841-752
venlafaxine hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	Bryant Ranch Prepack	71335-1338
venlafaxine hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	Zydus Pharmaceuticals USA Inc.	68382-034
venlafaxine hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	Zydus Pharmaceuticals USA Inc.	68382-035
venlafaxine hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	A-S Medication Solutions	50090-6301
venlafaxine hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	Zydus Pharmaceuticals USA Inc.	68382-036
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 37.5 mg/1	Capsule, Extended releaseOral	Zydus Lifesciences Limited	70771-1836
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 75 mg/1	Capsule, Extended releaseOral	Zydus Lifesciences Limited	70771-1837
Venlafaxine Hydrochloride	Venlafaxine hydrochloride 150 mg/1	Capsule, Extended releaseOral	Zydus Lifesciences Limited	70771-1838