citalopram

Generic: citalopram

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2601
Product ID 70518-2601_4a69e716-1140-5ce8-e063-6394a90a57eb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077042
Listing Expiration 2027-12-31
Marketing Start 2020-02-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182601
Hyphenated Format 70518-2601

Supplemental Identifiers

RxCUI
309314
UNII
I1E9D14F36

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 (source: ndc)
Generic Name citalopram (source: ndc)
Application Number ANDA077042 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX (70518-2601-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2601-2)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2601-3)
source: ndc

Packages (2)

70518-2601-1 100 POUCH in 1 BOX (70518-2601-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2601-2) 70518-2601-3 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2601-3)

Ingredients (1)

citalopram hydrobromide (40 mg/1)

Linked Drug Pages (1)

Citalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a69e716-1140-5ce8-e063-6394a90a57eb", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["aa9c1440-354f-43a6-9e70-fd7bafcb03c5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2601-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2601-2)", "package_ndc": "70518-2601-1", "marketing_start_date": "20200416"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2601-3)", "package_ndc": "70518-2601-3", "marketing_start_date": "20240416"}], "brand_name": "Citalopram", "product_id": "70518-2601_4a69e716-1140-5ce8-e063-6394a90a57eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2601", "generic_name": "citalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077042", "marketing_category": "ANDA", "marketing_start_date": "20200226", "listing_expiration_date": "20271231"}