BRIMONIDINE TARTRATE
NDC 70069-231, BRIMONIDINE TARTRATE, solution/ drops, from Somerset Therapeutics, LLC.
- Product NDC
- 70069-231
- Status
- Listed
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208992
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70069-231 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BRIMONIDINE TARTRATE2 mg/mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA]; alpha-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70069-231-01 | 70069023101 | 1 BOTTLE in 1 CARTON (70069-231-01) / 5 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cdb8620f-adfa-4433-b285-9c42334f8600NADAC price for package 70069023101
GET /v1/drugs/nadac/70069023101
Use it
Look up 70069-231 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70069-231 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70069-231. 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.