BRIMONIDINE TARTRATE
- Product NDC
- 70069-566
- 11-digit product format
- 700690566
- Labeler code
- 70069
- Product ID
- 70069-566_5a808f88-afeb-4ab3-b005-56b68b27dc7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BRIMONIDINE TARTRATE
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Somerset Therapeutics, LLC
- Application
- ANDA216906
- Marketing category
- ANDA
- Marketing start
- 2024-08-26
- Substance
- BRIMONIDINE TARTRATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BRIMONIDINE TARTRATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BRIMONIDINE TARTRATE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4S9CL2DY2H |
| Rxcui | 861204 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70069-566-01 | BRIMONIDINE TARTRATE | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 4 |
| 70069-566-01 | BRIMONIDINE TARTRATE | 5 mL in 1 BOTTLE | SOLUTION/ DROPS | 5 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70069-566 | BRIMONIDINE TARTRATE SOLUTION/ DROPS [SOMERSET THERAPEUTICS, LLC] | 4 | Current NDC, 2 package rows | 20240907_b8e108b3-aca8-4e3e-8577-37ac796148c3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70069-566-01 | 70069056601 | 1 BOTTLE in 1 CARTON (70069-566-01) / 5 mL in 1 BOTTLE | 1 bottle | 2024-08-26 | No | No | Historical |