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Tadalafil

NDC 82968-002, Tadalafil, tablet, film coated, from FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED.

Product NDC
82968-002
Status
Listed
Labeler
FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217606
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82968-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TADALAFIL5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
82968-002-018296800020130 TABLET, FILM COATED in 1 BOTTLE (82968-002-01)
82968-002-02829680002022 BLISTER PACK in 1 CARTON (82968-002-02) / 15 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0ea97208-5afc-4943-b35c-ea850203a794

Use it

Look up 82968-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82968-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82968-002. 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.