Brimonidine
- Product NDC
- 17478-715
- 11-digit product format
- 174780715
- Labeler code
- 17478
- Product ID
- 17478-715_edc8b30f-509f-44c1-b498-8cf9672aba66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Brimonidine Tartrate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Akorn
- Application
- ANDA076439
- Marketing category
- ANDA
- Marketing start
- 2006-09-07
- Marketing end
- 0000-00-00
- Substance
- BRIMONIDINE TARTRATE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17478-715-10 | Brimonidine | 5 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 5 | | 9 |
| 17478-715-10 | Brimonidine | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 9 |
| 17478-715-11 | Brimonidine | 10 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 10 | | 9 |
| 17478-715-11 | Brimonidine | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 9 |
| 17478-715-12 | Brimonidine | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | | 9 |
| 17478-715-12 | Brimonidine | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 9 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| Brimonidine Tartrate | ACTIVE INGREDIENT | 4S9CL2DY2H | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Brimonidine | ACTIVE MOIETY | E6GNX3HHTE | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Benzalkonium Chloride | INACTIVE INGREDIENT | F5UM2KM3W7 | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Citric Acid Monohydrate | INACTIVE INGREDIENT | 2968PHW8QP | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Hydrochloric Acid | INACTIVE INGREDIENT | QTT17582CB | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Polyvinyl Alcohol | INACTIVE INGREDIENT | 532B59J990 | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Sodium Chloride | INACTIVE INGREDIENT | 451W47IQ8X | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Sodium Citrate | INACTIVE INGREDIENT | 1Q73Q2JULR | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Sodium Hydroxide | INACTIVE INGREDIENT | 55X04QC32I | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN, INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-715 | BRIMONIDINE (BRIMONIDINE TARTRATE) SOLUTION/ DROPS [AKORN] | 9 | Legacy NDC, 6 package rows | 20220805_1ce6d79a-32c1-44dc-b50c-ada8848f39c3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-715-10 | 17478071510 | 1 BOTTLE, DROPPER in 1 CARTON (17478-715-10) > 5 mL in 1 BOTTLE, DROPPER | 2006-09-07 | 0000-00-00 | No | No | Current |
| 17478-715-11 | 17478071511 | 1 BOTTLE, DROPPER in 1 CARTON (17478-715-11) > 10 mL in 1 BOTTLE, DROPPER | 2006-09-07 | 0000-00-00 | No | No | Current |
| 17478-715-12 | 17478071512 | 1 BOTTLE, DROPPER in 1 CARTON (17478-715-12) > 15 mL in 1 BOTTLE, DROPPER | 2006-09-07 | 0000-00-00 | No | No | Current |