United States · FDA National Drug Code directory
Hydrocodone Bitartrate and Acetaminophen
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 27808-037_cf89ef14-b1bb-4341-8911-892ce7d157c1
- Product NDC
- 27808-037
- Form
- TABLET
- Composition / generic term
- Hydrocodone Bitartrate and Acetaminophen
- Labeler
- Cranbury Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141006
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCODONE BITARTRATE — 10 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (27808-037-01) · 27808-037-01
- 500 TABLET in 1 BOTTLE, PLASTIC (27808-037-02) · 27808-037-02
- 1000 TABLET in 1 BOTTLE, PLASTIC (27808-037-03) · 27808-037-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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