United States · FDA National Drug Code directory
Tamiflu
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
- 0004-0800_94a312ac-c47a-4437-8dd3-6bcd7e08e42c
- Product NDC
- 0004-0800
- Form
- CAPSULE
- Composition / generic term
- oseltamivir phosphate
- Labeler
- Genentech, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 19991027
- Source listing expiry
- 20261231
Source-listed ingredients
- OSELTAMIVIR PHOSPHATE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (0004-0800-07) / 10 CAPSULE in 1 BOTTLE, PLASTIC · 0004-0800-07
- 1 BLISTER PACK in 1 CARTON (0004-0800-85) / 10 CAPSULE in 1 BLISTER PACK · 0004-0800-85
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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