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Sildenafil Citrate

NDC 70771-1668, Sildenafil Citrate, powder, for suspension, from Zydus Lifesciences Limited.

Product NDC
70771-1668
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215708
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1668 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SILDENAFIL CITRATE10 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
70771-1668-4707711668041 BOTTLE, GLASS in 1 CARTON (70771-1668-4) / 112 mL in 1 BOTTLE, GLASS
70771-1668-5707711668051 BOTTLE, PLASTIC in 1 CARTON (70771-1668-5) / 112 mL in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ef4d02f-76ee-4f67-9f4f-1cd554decb31

Use it

Look up 70771-1668 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1668 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1668. 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.