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BETAMETHASONE DIPROPIONATE

NDC 59651-699, BETAMETHASONE DIPROPIONATE, ointment, augmented, from Aurobindo Pharma Limited.

Product NDC
59651-699
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
OINTMENT, AUGMENTED
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218289
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-699 \
  -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
59651-699-14596510699141 TUBE in 1 CARTON (59651-699-14) / 15 g in 1 TUBE
59651-699-46596510699461 TUBE in 1 CARTON (59651-699-46) / 45 g in 1 TUBE
59651-699-50596510699501 TUBE in 1 CARTON (59651-699-50) / 50 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e0e0baea-1744-4708-bda7-4ab7783a3fb4

Use it

Look up 59651-699 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-699 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-699. 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.