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Nadolol

NDC 70771-1089, Nadolol, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1089
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207761
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1089 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NADOLOL20 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
70771-1089-0707711089001000 TABLET in 1 BOTTLE (70771-1089-0)
70771-1089-170771108901100 TABLET in 1 BOTTLE (70771-1089-1)
70771-1089-47077110890410 BLISTER PACK in 1 CARTON (70771-1089-4) / 1 TABLET in 1 BLISTER PACK (70771-1089-2)
70771-1089-97077110890990 TABLET in 1 BOTTLE (70771-1089-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/29433c5a-51c6-4fb9-9174-1b1c616c9e57

Use it

Look up 70771-1089 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1089 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1089. 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.