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Sildenafil

NDC 65862-688, Sildenafil, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-688
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203963
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-688 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SILDENAFIL CITRATE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
65862-688-906586206889090 TABLET, FILM COATED in 1 BOTTLE (65862-688-90)
65862-688-99658620688991000 TABLET, FILM COATED in 1 BOTTLE (65862-688-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/17621e92-79a0-46aa-86c7-ea179e81928d

  • NADAC price for package 65862068890

    GET /v1/drugs/nadac/65862068890

  • NADAC price for package 65862068899

    GET /v1/drugs/nadac/65862068899

Use it

Look up 65862-688 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-688 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-688. 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.