Valacyclovir Hydrochloride
NDC 71335-0708, Valacyclovir Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-0708
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090682
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0708 \ -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 |
|---|---|---|
| 71335-0708-0 | 71335070800 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0) |
| 71335-0708-1 | 71335070801 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0708-1) |
| 71335-0708-2 | 71335070802 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0708-2) |
| 71335-0708-3 | 71335070803 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-0708-3) |
| 71335-0708-4 | 71335070804 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0708-4) |
| 71335-0708-5 | 71335070805 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0708-5) |
| 71335-0708-6 | 71335070806 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6) |
| 71335-0708-7 | 71335070807 | 8 TABLET, FILM COATED in 1 BOTTLE (71335-0708-7) |
| 71335-0708-8 | 71335070808 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0708-8) |
| 71335-0708-9 | 71335070809 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0708-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/93dccd99-d28b-4c47-872c-c3c0001b8a7f
Use it
Look up 71335-0708 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0708 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0708. 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.