Sildenafil Citrate
NDC 67877-648, Sildenafil Citrate, powder, for suspension, from Ascend Laboratories, LLC.
- Product NDC
- 67877-648
- Status
- Listed
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212440
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/67877-648 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SILDENAFIL CITRATE10 mg/mL
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC]; Phosphodiesterase 5 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 67877-648-11 | 67877064811 | 1 BOTTLE, GLASS in 1 CARTON (67877-648-11) / 112 mL in 1 BOTTLE, GLASS |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a0fa4162-e1b7-4293-ab7d-c5b375779060
Use it
Look up 67877-648 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67877-648 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67877-648. 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.