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Sulfacetamide Sodium and Prednisolone Sodium Phosphate

NDC 68071-1650, Sulfacetamide Sodium and Prednisolone Sodium Phosphate, solution/ drops, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-1650
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074449
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1650 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFACETAMIDE SODIUM100 mg/mL
  • PREDNISOLONE SODIUM PHOSPHATE2.3 mg/mL

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]

Package NDCNDC-11Package
68071-1650-5680711650055 mL in 1 BOX (68071-1650-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/835def0b-ed5a-61a0-e053-2a91aa0ae7ae

Use it

Look up 68071-1650 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1650 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-1650. 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.