What is NDC 61919-882?

61919-882 is the product NDC for Desvenlafaxine ER, Desvenlafaxine succinate 50 mg/1 tablet, film coated, extended release, listed with the FDA by Direct_Rx. It has 3 package NDCs, shown above in 10- and 11-digit form.

Direct_Rx, NDC labeler code 61919. 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 ER?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Desvenlafaxine ER NDC 61919-882 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)61919-882Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61919-0882Add 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
61919-882-28	6191908822861919088228	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-28)Marketed from Jun 4, 2019
61919-882-30	6191908823061919088230	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-30)Marketed from Jun 4, 2019
61919-882-60	6191908826061919088260	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-60)Marketed from Jun 4, 2019

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 ER
Generic name (nonproprietary): desvenlafaxine er
Active ingredients: Desvenlafaxine succinate — 50 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: Direct_RxNDC labeler code 61919
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204172
Marketing start: Jun 4, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 2D6 Inhibitors (Mechanism)Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 61919-882_4c49ea72-e09e-fa7c-e063-6294a90aba89SPL ID 4c49ea72-e09e-fa7c-e063-6294a90aba89SPL set ID 8a834c66-846e-38a8-e053-2a95a90a4035RxCUI 1874559UNII ZB22ENF0XR
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

N461919088228 followed by a unit qualifier and the quantity

Package 61919-0882-28. 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 Mar 5, 2026.

Indications (excerpt from the label)

Desvenlafaxine extended-release tablet is indicated for the treatment of adults with major depressive disorder (MDD) [see CLINICAL STUDIES (14)].

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61919-882

What is NDC 61919-882?: 61919-882 is the product NDC for Desvenlafaxine ER, Desvenlafaxine succinate 50 mg/1 tablet, film coated, extended release, listed with the FDA by Direct_Rx. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Desvenlafaxine ER.
What is the active ingredient?: Desvenlafaxine succinate.
Who is the labeler?: Direct_Rx, NDC labeler code 61919. 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 ER?: 1 other product NDC are listed under this name. See all Desvenlafaxine ER 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 ER NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Desvenlafaxine ER	Desvenlafaxine succinate 50 mg/1	Tablet, Extended releaseOral	Direct_rx	72189-567	72189-0567-2872189-0567-3072189-0567-60

Other NDCs under ANDA 204172

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

FDA NDC Directory listings under ANDA 204172
Product	Strength	Form · route	Labeler	Product NDC
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-6894
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-7468
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-592
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-593
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-604
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8556
Desvenlafaxine Succinate	Desvenlafaxine succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-1150
Desvenlafaxine Succinate	Desvenlafaxine succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-1331
Desvenlafaxine Succinate	Desvenlafaxine succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-2494