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Nateglinide

NDC 70771-1016, Nateglinide, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1016
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205248
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1016 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NATEGLINIDE120 mg/1

Pharmacologic classes

Glinide [EPC]; Potassium Channel Antagonists [MoA]

Package NDCNDC-11Package
70771-1016-0707711016001000 TABLET, FILM COATED in 1 BOTTLE (70771-1016-0)
70771-1016-170771101601100 TABLET, FILM COATED in 1 BOTTLE (70771-1016-1)
70771-1016-37077110160330 TABLET, FILM COATED in 1 BOTTLE (70771-1016-3)
70771-1016-47077110160410 BLISTER PACK in 1 CARTON (70771-1016-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1016-2)
70771-1016-570771101605500 TABLET, FILM COATED in 1 BOTTLE (70771-1016-5)
70771-1016-97077110160990 TABLET, FILM COATED in 1 BOTTLE (70771-1016-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a82817dd-f8c4-4172-ba86-63c2beef456a

Use it

Look up 70771-1016 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1016 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1016. 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.