What is NDC 51655-667?

51655-667 is the product NDC for Citalopram, Citalopram hydrobromide 40 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Citalopram?

91 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Citalopram NDC 51655-667 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51655-667Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51655-0667Add 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
51655-667-26	5165506672651655066726	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-667-26)Marketed from Jan 13, 2021
51655-667-52	5165506675251655066752	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-667-52)Marketed from Jan 12, 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): Citalopram
Generic name (nonproprietary): citalopram
Active ingredients: Citalopram hydrobromide — 40 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Northwind Health Company, LLCNDC labeler code 51655
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078216
Marketing start: Jan 12, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 51655-667_4aa1bc4e-124f-a39b-e063-6394a90ae6b9SPL ID 4aa1bc4e-124f-a39b-e063-6394a90ae6b9SPL set ID a7ef6ad2-5f22-4ac7-b57a-f498bcb53be1RxCUI 200371, 309314UNII I1E9D14F36
Pharmacologic class: Serotonin 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

N451655066726 followed by a unit qualifier and the quantity

Package 51655-0667-26. 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 1, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Citalopram tablets are indicated for the treatment of major depressive disorder (MDD) in adults [see Clinical Studies ( 14 )] . Citalopram is a selective serotonin reuptake inhibitor (SSRI) indicated for the treatment of major depressive disorder (MDD) in adults ( 1 ) .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51655-667

What is NDC 51655-667?: 51655-667 is the product NDC for Citalopram, Citalopram hydrobromide 40 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Citalopram.
What is the active ingredient?: Citalopram hydrobromide.
Who is the labeler?: Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Citalopram?: 91 other product NDCs are listed under this name. See all Citalopram 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 Citalopram NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Citalopram	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0113	67046-0113-03
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0793	67046-0793-03
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0795	67046-0795-03
Citalopram	Citalopram hydrobromide 30 mg/1	CapsuleOral	Aurobindo Pharma Limited	59651-964	59651-0964-30
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0557	80425-0557-0180425-0557-0280425-0557-03
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4476	70518-4476-0070518-4476-01
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4416	70518-4416-00
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4335	70518-4335-0070518-4335-0170518-4335-02+1 more
Citalopramcitalopram hydrobromide	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4334	70518-4334-0070518-4334-02
Citalopramcitalopram hydrobromide	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4114	70518-4114-01

All 92 Citalopram NDCs

Other NDCs under ANDA 078216

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

FDA NDC Directory listings under ANDA 078216
Product	Strength	Form · route	Labeler	Product NDC
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-3349
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-3329
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-1830
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	Proficient Rx LP	63187-203
Citalopram	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0113
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-1906
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/1	TabletOral	Proficient Rx LP	63187-220
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-481
Citalopram	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	ASCLEMED USA INC.	87063-221
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4476
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-2198
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-0238
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-5132
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-043
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	A-S Medication Solutions	50090-6846
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals, Inc.	68788-0802
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-683
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	QPharma, Inc.	42708-091
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Torrent Pharmaceuticals Limited	13668-009
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	Torrent Pharmaceuticals Limited	13668-010

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