What is NDC 46708-152?

46708-152 is the product NDC for Desvenlafaxine, Desvenlafaxine 50 mg/1 tablet, extended release, listed with the FDA by Alembic Pharmaceuticals Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Alembic Pharmaceuticals Limited, NDC labeler code 46708. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Desvenlafaxine?

52 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Desvenlafaxine NDC 46708-152 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)46708-152Labeler and product segments. Claims need a package NDC.

Product NDC at billing width46708-0152Add 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
46708-152-30	4670801523046708015230	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-152-30)Marketed from Mar 5, 2013
46708-152-90	4670801529046708015290	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-152-90)Marketed from Mar 5, 2013

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): Desvenlafaxine
Generic name (nonproprietary): desvenlafaxine
Active ingredients: Desvenlafaxine — 50 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Alembic Pharmaceuticals LimitedNDC labeler code 46708
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 204150
Marketing start: Mar 5, 2013
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 2D6 Inhibitors (Mechanism)Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 46708-152_6ebe192e-2b88-43fc-a2c8-db2c42bc5a43SPL ID 6ebe192e-2b88-43fc-a2c8-db2c42bc5a43SPL set ID 9f74708c-6f6a-46cf-8c79-87a25c2bb6f8RxCUI 790264, 790288UNII NG99554ANWUPC 0346708152307, 0346708153304
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

N446708015230 followed by a unit qualifier and the quantity

Package 46708-0152-30. 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 Jan 27, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

Desvenlafaxine, a serotonin and norepinephrine reuptake inhibitor (SNRI), is indicated for the treatment of major depressive disorder (MDD) [see Clinical Studies (14) and Dosage and Administration (2.1)] . The efficacy of desvenlafaxine has been established in four short-term (8-week, placebo-controlled studies) of outpatients who met DSM-IV criteria for major depressive disorder. Desvenlafaxine is a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of major depressive disorder (MDD) (1).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 46708-152

What is NDC 46708-152?: 46708-152 is the product NDC for Desvenlafaxine, Desvenlafaxine 50 mg/1 tablet, extended release, listed with the FDA by Alembic Pharmaceuticals Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Desvenlafaxine.
What is the active ingredient?: Desvenlafaxine.
Who is the labeler?: Alembic Pharmaceuticals Limited, NDC labeler code 46708. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Desvenlafaxine?: 52 other product NDCs are listed under this name. See all Desvenlafaxine 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 Desvenlafaxine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Marlex Pharmaceuticals, Inc.	10135-821	10135-0821-1010135-0821-1410135-0821-30+1 more
Desvenlafaxine	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	Marlex Pharmaceuticals, Inc.	10135-822	10135-0822-1010135-0822-1410135-0822-30+1 more
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals, Inc.	68071-5332	68071-5332-03
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-555	72603-0555-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-556	72603-0556-0172603-0556-02
Desvenlafaxine	Desvenlafaxine succinate 100 mg/1	Tablet, Extended releaseOral	NorthStar Rx LLC	72603-557	72603-0557-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8760	68788-8760-0168788-8760-0368788-8760-06+1 more
Desvenlafaxine	Desvenlafaxine succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7190	50090-7190-0050090-7190-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7737	50090-7737-0050090-7737-01
Desvenlafaxine	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-3790	68071-3790-03

All 53 Desvenlafaxine NDCs

Other NDCs under NDA 204150

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

FDA NDC Directory listings under NDA 204150
Product	Strength	Form · route	Labeler	Product NDC
Desvenlafaxine	Desvenlafaxine 100 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-153
Desvenlafaxine	Desvenlafaxine 50 mg/1	Tablet, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	63304-191
Desvenlafaxine	Desvenlafaxine 100 mg/1	Tablet, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	63304-192