Brinzolamide
- Product NDC
- 63629-8793
- 11-digit product format
- 636298793
- Labeler code
- 63629
- Product ID
- 63629-8793_d0882b87-311e-49a7-aa12-2ec4a28b4e3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Brinzolamide
- Dosage form
- SUSPENSION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020816
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-03-08
- Marketing end
- 0000-00-00
- Substance
- BRINZOLAMIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8793 | BRINZOLAMIDE SUSPENSION/ DROPS [BRYANT RANCH PREPACK] | 102 | Legacy NDC | 20240112_cd9837a8-5c50-4343-8f66-b8c6403a6f0d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8793-1 | 63629879301 | 1 BOTTLE, PLASTIC in 1 CARTON (63629-8793-1) > 10 mL in 1 BOTTLE, PLASTIC | 2021-09-09 | 0000-00-00 | No | No | Current |