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Bupropion Hydrochloride XL

NDC 70436-011, bupropion hydrochloride, tablet, extended release, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-011
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210015
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-011 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE300 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
70436-011-0270436001102500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-02)
70436-011-047043600110430 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-04)
70436-011-067043600110690 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/06d4d890-11ed-4f31-8778-c73432e3ea69

Use it

Look up 70436-011 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-011 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-011. 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.