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TRAMADOL HYDROCHLORIDE

NDC 27808-301, TRAMADOL HYDROCHLORIDE, tablet, film coated, from Cranbury Pharmaceuticals, LLC.

Product NDC
27808-301
Status
Listed
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091498
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/27808-301 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRAMADOL HYDROCHLORIDE50 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
27808-301-0127808030101100 TABLET, FILM COATED in 1 BOTTLE (27808-301-01)
27808-301-0227808030102500 TABLET, FILM COATED in 1 BOTTLE (27808-301-02)
27808-301-03278080301031000 TABLET, FILM COATED in 1 BOTTLE (27808-301-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1d4af58f-17f3-4cbd-870c-098ace954872

Use it

Look up 27808-301 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27808-301 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27808-301. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.