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VARDENAFIL

NDC 70771-1049, VARDENAFIL, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1049
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208960
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1049 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VARDENAFIL HYDROCHLORIDE TRIHYDRATE10 mg/1

Pharmacologic classes

Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]

Package NDCNDC-11Package
70771-1049-170771104901100 TABLET, FILM COATED in 1 BOTTLE (70771-1049-1)
70771-1049-37077110490330 TABLET, FILM COATED in 1 BOTTLE (70771-1049-3)
70771-1049-97077110490990 TABLET, FILM COATED in 1 BOTTLE (70771-1049-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8ea14f7e-44a0-4d9c-968a-87b97ca12f09

Use it

Look up 70771-1049 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1049 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1049. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.