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Nateglinide

NDC 70771-1015, Nateglinide, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1015
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/70771-1015 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NATEGLINIDE60 mg/1

Pharmacologic classes

Glinide [EPC]; Potassium Channel Antagonists [MoA]

Package NDCNDC-11Package
70771-1015-0707711015001000 TABLET, FILM COATED in 1 BOTTLE (70771-1015-0)
70771-1015-170771101501100 TABLET, FILM COATED in 1 BOTTLE (70771-1015-1)
70771-1015-37077110150330 TABLET, FILM COATED in 1 BOTTLE (70771-1015-3)
70771-1015-47077110150410 BLISTER PACK in 1 CARTON (70771-1015-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1015-2)
70771-1015-570771101505500 TABLET, FILM COATED in 1 BOTTLE (70771-1015-5)
70771-1015-97077110150990 TABLET, FILM COATED in 1 BOTTLE (70771-1015-9)

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 70771-1015 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1015 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1015. 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.