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
- 87063-050_4ca4b03b-efbe-4d32-e063-6394a90af0f3
- Product NDC
- 87063-050
- Form
- TABLET
- Composition / generic term
- Hydrocodone Bitartrate and Acetaminophen
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180713
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROCODONE BITARTRATE — 7.5 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (87063-050-01) · 87063-050-01
- 5 TABLET in 1 BOTTLE (87063-050-05) · 87063-050-05
- 7 TABLET in 1 BOTTLE (87063-050-07) · 87063-050-07
- 10 TABLET in 1 BOTTLE (87063-050-10) · 87063-050-10
- 14 TABLET in 1 BOTTLE (87063-050-14) · 87063-050-14
- 20 TABLET in 1 BOTTLE (87063-050-20) · 87063-050-20
- 30 TABLET in 1 BOTTLE (87063-050-30) · 87063-050-30
- 60 TABLET in 1 BOTTLE (87063-050-60) · 87063-050-60
- 90 TABLET in 1 BOTTLE (87063-050-90) · 87063-050-90
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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