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Hydrocodone Bitartrate and Acetaminophen

NDC 27808-049, Hydrocodone Bitartrate and Acetaminophen, solution, from Cranbury Pharmaceuticals, LLC.

Product NDC
27808-049
Status
Listed
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201295
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/27808-049 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE7.5 mg/15mL
  • ACETAMINOPHEN325 mg/15mL

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
27808-049-0127808004901473 mL in 1 BOTTLE, PLASTIC (27808-049-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/57e1fe79-eb60-4f4f-bb38-6df0270d408f

Use it

Look up 27808-049 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27808-049 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27808-049. 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.