Tamsulosin Hydrochloride
NDC 70518-2052, Tamsulosin Hydrochloride, capsule, from REMEDYREPACK INC..
- Product NDC
- 70518-2052
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202433
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2052 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TAMSULOSIN HYDROCHLORIDE.4 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA]; alpha-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-2052-0 | 70518205200 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-0) |
| 70518-2052-1 | 70518205201 | 30 CAPSULE in 1 BLISTER PACK (70518-2052-1) |
| 70518-2052-3 | 70518205203 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-3) |
| 70518-2052-4 | 70518205204 | 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-4) |
| 70518-2052-5 | 70518205205 | 50 POUCH in 1 BOX (70518-2052-5) / 1 CAPSULE in 1 POUCH (70518-2052-6) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a608ddc8-fe42-484e-b61f-307c60151138
Use it
Look up 70518-2052 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2052 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2052. 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.