BRIMONIDINE TARTRATE 0.25% / POTASSIUM AZELOYL DIGLYCINATE 8%
- Product NDC
- 72934-1027
- 11-digit product format
- 729341027
- Labeler code
- 72934
- Product ID
- 72934-1027_88ef2cc1-1856-9606-e053-2995a90a2e67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BRIMONIDINE TARTRATE 0.25% / POTASSIUM AZELOYL DIGLYCINATE 8%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sincerus Florida, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-05-16
- Marketing end
- 0000-00-00
- Substance
- BRIMONIDINE TARTRATE
- Active strength
- 0 g/100g
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 72934-1027-2 | BRIMONIDINE TARTRATE 0.25% / POTASSIUM AZELOYL DIGLYCINATE 8% | 30 g in 1 BOTTLE, PUMP | GEL | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72934-1027 | BRIMONIDINE TARTRATE 0.25% / POTASSIUM AZELOYL DIGLYCINATE 8% GEL [SINCERUS FLORIDA, LLC] | 1 | Legacy NDC, 1 package rows | 20190516_88ef2cc1-1855-9606-e053-2995a90a2e67.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72934-1027-2 | 72934102702 | 30 g in 1 BOTTLE, PUMP | 30 g | Historical |