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Citalopram Hydrobromide

NDC 68071-1906, Citalopram Hydrobromide, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-1906
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078216
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1906 \
  -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
68071-1906-36807119060330 TABLET in 1 BOTTLE (68071-1906-3)
68071-1906-66807119060660 TABLET in 1 BOTTLE (68071-1906-6)
68071-1906-96807119060990 TABLET in 1 BOTTLE (68071-1906-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/579836d8-64ed-de2d-e053-2a91aa0a8392

Use it

Look up 68071-1906 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1906 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-1906. 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.