United States · FDA National Drug Code directory
Terbutaline Sulfate
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
- 62559-722_ee722f8c-05d6-43bc-825d-9496579032c4
- Product NDC
- 62559-722
- Form
- TABLET
- Composition / generic term
- Terbutaline Sulfate
- Labeler
- ANI Pharmaceuticals, Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20181016
- Source listing expiry
- 20261231
Source-listed ingredients
- TERBUTALINE SULFATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (62559-722-01) · 62559-722-01
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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