What is NDC 17856-0564?

17856-0564 is the product NDC for Citalopram Hydrobromide, Citalopram hydrobromide 10 mg/5mL solution, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 1 package NDC, shown above in 10- and 11-digit form.

ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. 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 17856-0564

NDC codes

FDA NDC Directory

Product NDC (as listed)17856-0564Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17856-0564Add 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
17856-0564-1	1785605640117856056401	72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0564-1) / 10 mL in 1 CUP, UNIT-DOSEMarketed from Jun 5, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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/5mL
Dosage form: Solution
Route: Oral
Labeler: ATLANTIC BIOLOGICALS CORP.NDC labeler code 17856
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 201450
Marketing start: May 31, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 17856-0564_34f3a909-1a50-3667-e063-6294a90aa4aaSPL ID 34f3a909-1a50-3667-e063-6294a90aa4aaSPL set ID 2640311d-8b88-4513-9c80-a08390b8142aRxCUI 309313UNII 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

N417856056401 followed by a unit qualifier and the quantity

Package 17856-0564-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 17856-0564

What is NDC 17856-0564?: 17856-0564 is the product NDC for Citalopram Hydrobromide, Citalopram hydrobromide 10 mg/5mL solution, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 1 package NDC, 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?: ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. 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 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 201450

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

FDA NDC Directory listings under ANDA 201450
Product	Strength	Form · route	Labeler	Product NDC
Citalopram Hydrobromide	Citalopram hydrobromide 10 mg/5mL	SolutionOral	Camber Pharmaceuticals, Inc.	31722-564