United States · FDA National Drug Code directory
Rizatriptan Benzoate
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
- 71335-1912_31217a32-abec-47de-b4ec-bf2205931ffb
- Product NDC
- 71335-1912
- Form
- TABLET
- Composition / generic term
- Rizatriptan Benzoate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121231
- Source listing expiry
- 20261231
Source-listed ingredients
- RIZATRIPTAN BENZOATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BLISTER PACK (71335-1912-1) · 71335-1912-1
- 6 TABLET in 1 BLISTER PACK (71335-1912-2) · 71335-1912-2
- 90 TABLET in 1 BLISTER PACK (71335-1912-3) · 71335-1912-3
- 9 TABLET in 1 BLISTER PACK (71335-1912-4) · 71335-1912-4
- 30 TABLET in 1 BLISTER PACK (71335-1912-5) · 71335-1912-5
- 18 TABLET in 1 BLISTER PACK (71335-1912-6) · 71335-1912-6
- 12 TABLET in 1 BLISTER PACK (71335-1912-7) · 71335-1912-7
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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