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Levonorgestrel

NDC 51660-999, Levonorgestrel, tablet, from Ohm Laboratories Inc..

Product NDC
51660-999
Status
Listed
Labeler
Ohm Laboratories Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA202635
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51660-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVONORGESTREL1.5 mg/1

Pharmacologic classes

Inhibit Ovum Fertilization [PE]; Progesterone Congeners [CS]; Progesterone Congeners [CS]; Progestin [EPC]; Progestin-containing Intrauterine System [EPC]

Package NDCNDC-11Package
51660-999-01516600999011 BLISTER PACK in 1 CARTON (51660-999-01) / 1 TABLET in 1 BLISTER PACK
51660-999-11516600999111 BLISTER PACK in 1 CARTON (51660-999-11) / 1 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 51660099901

    GET /v1/drugs/nadac/51660099901

Use it

Look up 51660-999 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51660-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51660-999. 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.