United States · FDA National Drug Code directory
Atovaquone and Proguanil Hydrochloride
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
- 71335-3160_fc935266-98cd-4a37-9b59-bdc6f0910b80
- Product NDC
- 71335-3160
- Form
- TABLET, FILM COATED
- Composition / generic term
- Atovaquone and Proguanil Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110915
- Source listing expiry
- 20271231
Source-listed ingredients
- ATOVAQUONE — 250 mg/1
- PROGUANIL HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-3160-1) · 71335-3160-1
- 24 TABLET, FILM COATED in 1 BOTTLE (71335-3160-2) · 71335-3160-2
- 5 TABLET, FILM COATED in 1 BOTTLE (71335-3160-3) · 71335-3160-3
- 12 TABLET, FILM COATED in 1 BOTTLE (71335-3160-4) · 71335-3160-4
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-3160-5) · 71335-3160-5
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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