What is NDC 67877-728?

67877-728 is the product NDC for Venlafaxine, Venlafaxine hydrochloride 150 mg/1 tablet, extended release, listed with the FDA by Ascend Laboratories, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Ascend Laboratories, LLC, NDC labeler code 67877. 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 67877-728 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67877-728Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67877-0728Add 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
67877-728-30	6787707283067877072830	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-728-30)Marketed from Jun 11, 2021
67877-728-90	6787707289067877072890	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-728-90)Marketed from Jun 11, 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 — 150 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Ascend Laboratories, LLCNDC labeler code 67877
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214127
Marketing start: Jun 11, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 67877-728_17943f8a-6ea6-4e86-93cc-df580774a8d9SPL ID 17943f8a-6ea6-4e86-93cc-df580774a8d9SPL set ID 528d5392-4ad5-48c5-963d-6ebfb9187db4RxCUI 808744, 808748, 808751, 808753UNII 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

N467877072830 followed by a unit qualifier and the quantity

Package 67877-0728-30. 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

Current FDA label (SPL), effective Jul 29, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Venlafaxine extended-release tablets are a selective serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for: Major Depressive Disorder (MDD) ( 1.1 ) Social Anxiety Disorder (SAD) ( 1.2 ) 1.1 Major Depressive Disorder Venlafaxine extended-release tablets (venlafaxine hydrochloride) are indicated for the treatment of major depressive disorder (MDD). Efficacy of venlafaxine in MDD was shown in both short-term trials and a longer-term trial in MDD [ see Clinical Studies (14.1)]. A major depressive episode (DSM-IV) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed mood or the loss of interest or pleasure in nearly all activities, represe…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67877-728

What is NDC 67877-728?: 67877-728 is the product NDC for Venlafaxine, Venlafaxine hydrochloride 150 mg/1 tablet, extended release, listed with the FDA by Ascend Laboratories, LLC. 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?: Ascend Laboratories, LLC, NDC labeler code 67877. 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 214127

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

FDA NDC Directory listings under ANDA 214127
Product	Strength	Form · route	Labeler	Product NDC
Venlafaxine	Venlafaxine hydrochloride 37.5 mg/1	Tablet, Extended releaseOral	Ascend Laboratories, LLC	67877-726
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	Tablet, Extended releaseOral	Ascend Laboratories, LLC	67877-727
Venlafaxine	Venlafaxine hydrochloride 225 mg/1	Tablet, Extended releaseOral	Ascend Laboratories, LLC	67877-729
Venlafaxine	Venlafaxine hydrochloride 75 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-3820
Venlafaxine	Venlafaxine hydrochloride 150 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4500