NDC codes

FDA NDC Directory
Product NDC (as listed)31722-124Labeler and product segments. Claims need a package NDC.
Product NDC at billing width31722-0124Add 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
31722-124-303172201243030 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-124-30)Marketed from Oct 23, 2020
31722-124-903172201249090 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-124-90)Marketed from Oct 23, 2020

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
Active ingredients
Venlafaxine hydrochloride75 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214419
Marketing start
Listing expires
Other FDA classes
Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 31722-124_495259b8-9f81-4b6e-aa51-d199aa0edfb8SPL ID 495259b8-9f81-4b6e-aa51-d199aa0edfb8SPL set ID 8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd3RxCUI 808744, 808748, 808751, 808753UNII 7D7RX5A8MOUPC 0331722126908, 0331722125307, 0331722126304, 0331722123907, 0331722123303, 0331722124300, 0331722124904, 0331722125901

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

N431722012430 followed by a unit qualifier and the quantity

Package 31722-0124-30. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 214419

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

FDA NDC Directory listings under ANDA 214419
ProductStrengthForm · routeLabelerProduct NDC
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 37.5 mg/1Tablet, Extended releaseOralCamber Pharmaceuticals, Inc.31722-123
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 75 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-497
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 37.5 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-496
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 225 mg/1Tablet, Extended releaseOralCamber Pharmaceuticals, Inc.31722-126
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 150 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-498
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 150 mg/1Tablet, Extended releaseOralCamber Pharmaceuticals, Inc.31722-125
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 225 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-499
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 75 mg/1Tablet, Extended releaseOralXLCare Pharmaceuticals, Inc.72865-198
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 37.5 mg/1Tablet, Extended releaseOralXLCare Pharmaceuticals, Inc.72865-197
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 150 mg/1Tablet, Extended releaseOralXLCare Pharmaceuticals, Inc.72865-199
Venlafaxine HydrochloridevenlafaxineVenlafaxine hydrochloride 225 mg/1Tablet, Extended releaseOralXLCare Pharmaceuticals, Inc.72865-200

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