Valacyclovir Hydrochloride
NDC 71335-1341, Valacyclovir Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-1341
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078518
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1341 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- VALACYCLOVIR HYDROCHLORIDE500 mg/1
Pharmacologic classes
DNA Polymerase Inhibitors [MoA]; Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]; Nucleoside Analog [EXT]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-1341-0 | 71335134100 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1341-0) |
| 71335-1341-1 | 71335134101 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1341-1) |
| 71335-1341-2 | 71335134102 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1341-2) |
| 71335-1341-3 | 71335134103 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-1341-3) |
| 71335-1341-4 | 71335134104 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1341-4) |
| 71335-1341-5 | 71335134105 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1341-5) |
| 71335-1341-6 | 71335134106 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1341-6) |
| 71335-1341-7 | 71335134107 | 8 TABLET, FILM COATED in 1 BOTTLE (71335-1341-7) |
| 71335-1341-8 | 71335134108 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1341-8) |
| 71335-1341-9 | 71335134109 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1341-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c28c069f-3b51-4474-aa38-1aed6b7b8678
Use it
Look up 71335-1341 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1341 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-1341. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.