DORZOLAMIDE HYDROCHLORIDE
- Product NDC
- 50090-5280
- 11-digit product format
- 500905280
- Labeler code
- 50090
- Product ID
- 50090-5280_143f3520-de82-4499-8b8d-14733e7b749d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dorzolamide hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA078981
- Marketing category
- ANDA
- Marketing start
- 2009-06-01
- Marketing end
- 0000-00-00
- Substance
- DORZOLAMIDE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5280-0 | 50090528000 | 10 mL in 1 BOTTLE (50090-5280-0) | 10 ml | 2020-10-21 | 0000-00-00 | No | No | Current |