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betamethasone dipropionate

NDC 70771-1550, betamethasone dipropionate, ointment, from Zydus Lifesciences Limited.

Product NDC
70771-1550
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
OINTMENT
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214048
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1550 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BETAMETHASONE DIPROPIONATE.5 mg/g

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
70771-1550-1707711550011 TUBE in 1 CARTON (70771-1550-1) / 15 g in 1 TUBE
70771-1550-4707711550041 TUBE in 1 CARTON (70771-1550-4) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f531da27-2435-49a3-8992-c65240c6a7fe

Use it

Look up 70771-1550 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1550 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1550. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.