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Hydrocodone Bitartrate and Acetaminophen

NDC 27808-115, Hydrocodone Bitartrate and Acetaminophen, tablet, from Cranbury Pharmaceuticals, LLC.

Product NDC
27808-115
Status
Listed
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202214
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/27808-115 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE7.5 mg/1
  • ACETAMINOPHEN300 mg/1

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
27808-115-0127808011501100 TABLET in 1 BOTTLE (27808-115-01)
27808-115-0227808011502500 TABLET in 1 BOTTLE (27808-115-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d8fe4ae4-bd19-42eb-b74d-f302b3f914ee

  • NADAC price for package 27808011501

    GET /v1/drugs/nadac/27808011501

Use it

Look up 27808-115 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27808-115 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27808-115. 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.