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Tilia Fe

NDC 75907-086, NdAc and EE Tablets and Ferrous Fumarate Tablets, kit, from Dr. Reddy�s Laboratories Inc..

Product NDC
75907-086
Status
Listed
Labeler
Dr. Reddy�s Laboratories Inc.
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202962
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/75907-086 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
75907-086-28759070086281 BLISTER PACK in 1 PACKET (75907-086-28) / 1 KIT in 1 BLISTER PACK
75907-086-32759070086323 BLISTER PACK in 1 CARTON (75907-086-32) / 1 KIT in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/118fb017-b44d-4223-ac5a-501ca96de210
  • NADAC price for package 75907008628

    GET /v1/drugs/nadac/75907008628
  • NADAC price for package 75907008632

    GET /v1/drugs/nadac/75907008632

Use it

Look up 75907-086 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/75907-086 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 75907-086. 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.