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
- 70518-3436_5071b891-7d0a-23d6-e063-6294a90a4b33
- Product NDC
- 70518-3436
- Form
- CAPSULE
- Composition / generic term
- acyclovir
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220614
- Source listing expiry
- 20271231
Source-listed ingredients
- ACYCLOVIR — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BLISTER PACK (70518-3436-0) · 70518-3436-0
- 50 POUCH in 1 BOX (70518-3436-1) / 1 CAPSULE in 1 POUCH (70518-3436-2) · 70518-3436-1
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →