Premphase
NDC 0046-2575, conjugated estrogens and medroxyprogesterone acetate, kit, from Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
- Product NDC
- 0046-2575
- Status
- Listed
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA020527
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0046-2575 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0046-2575-12 | 00046257512 | 1 BLISTER PACK in 1 CARTON (0046-2575-12) / 1 KIT in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/fd0c0836-5d23-2183-da81-9dc7f4287052NADAC price for package 00046257512
GET /v1/drugs/nadac/00046257512
Use it
Look up 0046-2575 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0046-2575 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0046-2575. 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.