What is NDC 55700-787?

55700-787 is the product NDC for Citalopram Hydrobromide, Citalopram hydrobromide 10 mg/1 tablet, listed with the FDA by Quality Care Products, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Quality Care Products, LLC, NDC labeler code 55700. 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 55700-787

NDC codes

FDA NDC Directory

Product NDC (as listed)55700-787Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55700-0787Add 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
55700-787-30	5570007873055700078730	30 TABLET in 1 BOTTLE (55700-787-30)Marketed from Aug 30, 2019
55700-787-90	5570007879055700078790	90 TABLET in 1 BOTTLE (55700-787-90)Marketed from Aug 30, 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): Citalopram Hydrobromide
Generic name (nonproprietary): citalopram hydrobromide
Active ingredients: Citalopram hydrobromide — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Quality Care Products, LLCNDC labeler code 55700
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078216
Marketing start: Aug 30, 2019
Marketing end: Sep 30, 2027
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 55700-787_cace2491-2e54-4b8a-a5a3-682d282524ffSPL ID cace2491-2e54-4b8a-a5a3-682d282524ffSPL set ID e22fe468-5d9e-4ec7-a69b-4988e0b8acbdRxCUI 283672UNII 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

N455700078730 followed by a unit qualifier and the quantity

Package 55700-0787-30. 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 Dec 18, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Citalopram, is indicated for the treatment of depression. The efficacy of citalopram hydrobromide, in the treatment of depression was established in 4 to 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/…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55700-787

What is NDC 55700-787?: 55700-787 is the product NDC for Citalopram Hydrobromide, Citalopram hydrobromide 10 mg/1 tablet, listed with the FDA by Quality Care Products, LLC. It has 2 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?: Quality Care Products, LLC, NDC labeler code 55700. 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/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
Citalopram Hydrobromide	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals, Inc.	68788-0802	68788-0802-0168788-0802-0368788-0802-06+2 more

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 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

Showing 20 of 40.