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Bupropion Hydrochloride

NDC 71209-052, Bupropion Hydrochloride, tablet, film coated, from Cadila Pharmaceuticals Limited.

Product NDC
71209-052
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208606
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71209-052 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE75 mg/1

Pharmacologic classes

Aminoketone [EPC]; Dopamine Uptake Inhibitors [MoA]; Increased Dopamine Activity [PE]; Increased Norepinephrine Activity [PE]; Norepinephrine Uptake Inhibitors [MoA]

Package NDCNDC-11Package
71209-052-0571209005205100 TABLET, FILM COATED in 1 BOTTLE (71209-052-05)
71209-052-11712090052111000 TABLET, FILM COATED in 1 BOTTLE (71209-052-11)
71209-052-177120900521710 BLISTER PACK in 1 CARTON (71209-052-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/33210109-2ddb-4b0f-a45e-988e493ca628

Use it

Look up 71209-052 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-052 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-052. 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.