United States · FDA National Drug Code directory
acyclovir
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
- 71335-2261_1bed7dd6-b341-487f-8cdb-45c1d7906e32
- Product NDC
- 71335-2261
- Form
- CAPSULE
- Composition / generic term
- acyclovir
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190823
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE in 1 BOTTLE (71335-2261-0) · 71335-2261-0
- 30 CAPSULE in 1 BOTTLE (71335-2261-1) · 71335-2261-1
- 25 CAPSULE in 1 BOTTLE (71335-2261-2) · 71335-2261-2
- 35 CAPSULE in 1 BOTTLE (71335-2261-3) · 71335-2261-3
- 50 CAPSULE in 1 BOTTLE (71335-2261-4) · 71335-2261-4
- 100 CAPSULE in 1 BOTTLE (71335-2261-5) · 71335-2261-5
- 40 CAPSULE in 1 BOTTLE (71335-2261-6) · 71335-2261-6
- 60 CAPSULE in 1 BOTTLE (71335-2261-7) · 71335-2261-7
- 120 CAPSULE in 1 BOTTLE (71335-2261-8) · 71335-2261-8
- 20 CAPSULE in 1 BOTTLE (71335-2261-9) · 71335-2261-9
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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