citalopram hydrobromide

Generic: citalopram hydrobromide

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler camber pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

citalopram hydrobromide 10 mg/5mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-564
Product ID 31722-564_1285242d-4c02-8735-e063-6294a90aa6ad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201450
Listing Expiration 2026-12-31
Marketing Start 2015-12-21

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722564
Hyphenated Format 31722-564

Supplemental Identifiers

RxCUI
309313
UPC
0331722564243
UNII
I1E9D14F36

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name citalopram hydrobromide (source: ndc)
Generic Name citalopram hydrobromide (source: ndc)
Application Number ANDA201450 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/5mL
source: ndc
Packaging
  • 240 mL in 1 BOTTLE (31722-564-24)
source: ndc

Packages (1)

31722-564-24 240 mL in 1 BOTTLE (31722-564-24)

Ingredients (1)

citalopram hydrobromide (10 mg/5mL)

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1285242d-4c02-8735-e063-6294a90aa6ad", "openfda": {"upc": ["0331722564243"], "unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["dc7b3f88-ee55-4e3e-9ed4-fc06aa7620cc"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (31722-564-24)", "package_ndc": "31722-564-24", "marketing_start_date": "20151221"}], "brand_name": "Citalopram Hydrobromide", "product_id": "31722-564_1285242d-4c02-8735-e063-6294a90aa6ad", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "31722-564", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA201450", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}