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Citalopram Hydrobromide

NDC 68788-0802, Citalopram Hydrobromide, tablet, film coated, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-0802
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078216
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-0802 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CITALOPRAM HYDROBROMIDE20 mg/1

Pharmacologic classes

Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]

Package NDCNDC-11Package
68788-0802-168788080201100 TABLET, FILM COATED in 1 BOTTLE (68788-0802-1)
68788-0802-36878808020330 TABLET, FILM COATED in 1 BOTTLE (68788-0802-3)
68788-0802-66878808020660 TABLET, FILM COATED in 1 BOTTLE (68788-0802-6)
68788-0802-868788080208120 TABLET, FILM COATED in 1 BOTTLE (68788-0802-8)
68788-0802-96878808020990 TABLET, FILM COATED in 1 BOTTLE (68788-0802-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b52acd68-fed1-4680-9eaf-b72e7dcba6fb

Use it

Look up 68788-0802 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-0802 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-0802. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.