Norethindrone Acetate and Ethinyl Estradiol
NDC 68462-132, Norethindrone Acetate and Ethinyl Estradiol, tablet, from Glenmark Pharmaceuticals Inc., USA.
- Product NDC
- 68462-132
- Status
- Listed
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206969
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68462-132 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NORETHINDRONE ACETATE1 mg/1
- ETHINYL ESTRADIOL.02 mg/1
Pharmacologic classes
Estrogen Receptor Agonists [MoA]; Estrogen [EPC]; Progesterone Congeners [CS]; Progestin [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68462-132-81 | 68462013281 | 3 POUCH in 1 CARTON (68462-132-81) / 1 BLISTER PACK in 1 POUCH (68462-132-79) / 21 TABLET in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5a44f7a2-45f1-4d28-b9fb-61d9f2456422NADAC price for package 68462013281
GET /v1/drugs/nadac/68462013281
Use it
Look up 68462-132 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68462-132 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68462-132. 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.