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Loestrin 21 Day

NDC 51285-127, Norethindrone Acetate and Ethinyl Estradiol, tablet, from Teva Women's Health LLC.

Product NDC
51285-127
Status
Listed
Labeler
Teva Women's Health LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076381
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51285-127 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NORETHINDRONE ACETATE1.5 mg/1
  • ETHINYL ESTRADIOL30 ug/1

Pharmacologic classes

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

Package NDCNDC-11Package
51285-127-97512850127975 POUCH in 1 CARTON (51285-127-97) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f29ebcb5-7e65-4092-bfaa-f5ec026fc255

Use it

Look up 51285-127 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51285-127 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51285-127. 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.