betamethasone dipropionate
NDC 70771-1550, betamethasone dipropionate, ointment, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1550
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214048
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BETAMETHASONE DIPROPIONATE.5 mg/g
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1550-1 | 70771155001 | 1 TUBE in 1 CARTON (70771-1550-1) / 15 g in 1 TUBE |
| 70771-1550-4 | 70771155004 | 1 TUBE in 1 CARTON (70771-1550-4) / 45 g in 1 TUBE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f531da27-2435-49a3-8992-c65240c6a7fe
Use it
Look up 70771-1550 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1550. 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.