What is NDC 52427-632?

52427-632 is the product NDC for venlafaxine, Venlafaxine besylate monohydrate 112.5 mg/1 tablet, extended release, listed with the FDA by Almatica Pharma LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Venlafaxine besylate monohydrate.

Almatica Pharma LLC, NDC labeler code 52427. 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 52427-632 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)52427-632Labeler and product segments. Claims need a package NDC.

Product NDC at billing width52427-0632Add 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
52427-632-30	5242706323052427063230	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52427-632-30)Marketed from Aug 1, 2022

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 besylate monohydrate — 112.5 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Almatica Pharma LLCNDC labeler code 52427
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 215429
Marketing start: Jun 30, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 52427-632_e80091b4-ac1f-a50e-8ba3-54c794794928SPL ID e80091b4-ac1f-a50e-8ba3-54c794794928
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

N452427063230 followed by a unit qualifier and the quantity

Package 52427-0632-30. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 52427-632

What is NDC 52427-632?: 52427-632 is the product NDC for venlafaxine, Venlafaxine besylate monohydrate 112.5 mg/1 tablet, extended release, listed with the FDA by Almatica Pharma LLC. 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 besylate monohydrate.
Who is the labeler?: Almatica Pharma LLC, NDC labeler code 52427. 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