NDC codes

FDA NDC Directory
Product NDC (as listed)65841-753Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65841-0753Add 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 NDC11-digit (billing)PackageCopy
65841-753-066584107530630 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-06)Marketed from Jun 1, 2011
65841-753-10658410753101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-10)Marketed from Jun 1, 2011
65841-753-166584107531690 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-16)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 — 150 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090174
Marketing start
Listing expires
Other FDA classes
Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 65841-753_f20749dc-d1f6-4860-b583-82b82d3a2242SPL ID f20749dc-d1f6-4860-b583-82b82d3a2242SPL set ID 1be1be3a-304b-4e31-8732-335247029191RxCUI 313581, 313583, 313585UNII 7D7RX5A8MOUPC 0365841752106, 0365841753103

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

N465841075306 followed by a unit qualifier and the quantity

Package 65841-0753-06. 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 .

Full label on DailyMed (opens in a new tab)

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
ProductStrengthForm · routeLabelerProduct NDC
Venlafaxine HydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralPreferred Pharmaceuticals Inc.68788-8774
venlafaxine hydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralPreferred Pharmaceuticals Inc.68788-6806
venlafaxine hydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralNuCare Pharmaceuticals,Inc.68071-4442
venlafaxine hydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited65841-752
venlafaxine hydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited65841-751
venlafaxine hydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-034
venlafaxine hydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-035
venlafaxine hydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-036
Venlafaxine HydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited70771-1838
Venlafaxine HydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited70771-1836
Venlafaxine HydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited70771-1837
Venlafaxine HydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.70710-1699
Venlafaxine HydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.70710-1698
Venlafaxine HydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.70710-1700
venlafaxine hydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralA-S Medication Solutions50090-6301
venlafaxine hydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralBryant Ranch Prepack71335-1338

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venlafaxine hydrochloride NDC 65841-753 | Med-Code