What is NDC 63187-203?

63187-203 is the product NDC for Citalopram Hydrobromide, Citalopram hydrobromide 20 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 63187. 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 Hydrobromide?

28 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Citalopram Hydrobromide NDC 63187-203

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0203Add 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
63187-203-00	6318702030063187020300	100 TABLET in 1 BOTTLE (63187-203-00)Marketed from Nov 2, 2015
63187-203-30	6318702033063187020330	30 TABLET in 1 BOTTLE (63187-203-30)Marketed from Nov 2, 2015
63187-203-60	6318702036063187020360	60 TABLET in 1 BOTTLE (63187-203-60)Marketed from Nov 2, 2015
63187-203-72	6318702037263187020372	120 TABLET in 1 BOTTLE (63187-203-72)Marketed from Nov 2, 2015
63187-203-90	6318702039063187020390	90 TABLET in 1 BOTTLE (63187-203-90)Marketed from Nov 2, 2015

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 Hydrobromide
Generic name (nonproprietary): citalopram hydrobromide
Active ingredients: Citalopram hydrobromide — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 63187
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078216
Marketing start: Oct 18, 2007
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 63187-203_70196c8d-c1c0-457c-b9b2-dd1182416714SPL ID 70196c8d-c1c0-457c-b9b2-dd1182416714SPL set ID 1a136cc3-d655-4f3c-8710-2603dc008492RxCUI 200371, 283672UNII I1E9D14F36UPC 0363187220303, 0363187203900
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

N463187020300 followed by a unit qualifier and the quantity

Package 63187-0203-00. 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 Nov 1, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Citalopram HBr is indicated for the treatment of depression. The efficacy of citalopram HBr in the treatment of depression was established in 4-6 week, controlled trials of outpatients whose diagnosis corresponded most closely to the DSM-III and DSM-III-R category of major depressive disorder (see CLINICAL PHARMACOLOGY ). A major depressive episode (DSM-IV) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed or dysphoric mood that usually interferes with daily functioning, and includes at least five of the following nine symptoms: depressed mood, loss of interest in usual activities, significant change in weight and/or appetit…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-203

What is NDC 63187-203?: 63187-203 is the product NDC for Citalopram Hydrobromide, Citalopram hydrobromide 20 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Citalopram Hydrobromide.
What is the active ingredient?: Citalopram hydrobromide.
Who is the labeler?: Proficient Rx LP, NDC labeler code 63187. 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 Hydrobromide?: 28 other product NDCs are listed under this name. See all Citalopram Hydrobromide 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 Hydrobromide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0309	80425-0309-0180425-0309-0280425-0309-03
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-043	51655-0043-2651655-0043-52
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	TabletOral	Quality Care Products, LLC	55700-851	55700-0851-90
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/1	TabletOral	Quality Care Products, LLC	55700-787	55700-0787-3055700-0787-90
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/5mL	SolutionOral	ATLANTIC BIOLOGICALS CORP.	17856-0564	17856-0564-01
Citalopram Hydrobromidecitalopram	Citalopram hydrobromide 20 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-092	71610-0092-1571610-0092-3071610-0092-45+1 more
Citalopram Hydrobromidecitalopram	Citalopram hydrobromide 10 mg/1	TabletOral	Exelan Pharmaceuticals Inc.	76282-628	76282-0628-0576282-0628-1076282-0628-30+1 more
Citalopram Hydrobromidecitalopram	Citalopram hydrobromide 20 mg/1	TabletOral	Exelan Pharmaceuticals Inc.	76282-629	76282-0629-0576282-0629-1076282-0629-30+1 more
Citalopram Hydrobromide	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8962	68788-8962-0168788-8962-0368788-8962-06+2 more
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/5mL	SolutionOral	Camber Pharmaceuticals, Inc.	31722-564	31722-0564-24

All 29 Citalopram Hydrobromide 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	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
Citalopram	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	Torrent Pharmaceuticals Limited	13668-011

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