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Nortrel 21 Day

NDC 0555-9009, Norethindrone and Ethinyl Estradiol, tablet, from Teva Pharmaceuticals USA, Inc..

Product NDC
0555-9009
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072693
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0555-9009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NORETHINDRONE1 mg/1
  • ETHINYL ESTRADIOL.035 mg/1

Pharmacologic classes

Estrogen Receptor Agonists [MoA]; Estrogen [EPC]; Progesterone Congeners [CS]; Progestin [EPC]

Package NDCNDC-11Package
0555-9009-42005559009423 POUCH in 1 CARTON (0555-9009-42) / 1 BLISTER PACK in 1 POUCH (0555-9009-80) / 21 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/140c50d6-c931-423a-9aa0-526eae7ab93c

  • NADAC price for package 00555900942

    GET /v1/drugs/nadac/00555900942

Use it

Look up 0555-9009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0555-9009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0555-9009. 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.