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NDC 81968-351, solriamfetol, tablet, film coated, from Axsome Therapeutics, Inc..

Product NDC
81968-351
Status
Listed
Labeler
Axsome Therapeutics, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA211230
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81968-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SOLRIAMFETOL150 mg/1

Pharmacologic classes

Dopamine Uptake Inhibitors [MoA]; Dopamine and Norepinephrine Reuptake Inhibitor [EPC]; Norepinephrine Uptake Inhibitors [MoA]

Package NDCNDC-11Package
81968-351-018196803510130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81968-351-01)
81968-351-07819680351077 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)
81968-351-108196803511010 BLISTER PACK in 1 CARTON (81968-351-10) / 7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/362f206b-73e7-4009-8c34-5a9df55679ab

  • NADAC price for package 81968035101

    GET /v1/drugs/nadac/81968035101

Use it

Look up 81968-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81968-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81968-351. 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.