acetaZOLAMIDE
- Product NDC
- 68071-3632
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetaZOLAMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA211069
- Marketing category
- ANDA
- Substance
- ACETAZOLAMIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68071-3632-1 | 100 TABLET in 1 BOTTLE (68071-3632-1) | 2024-06-18 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| acetaZOLAMIDE Tablets, USP RX Only | NuCare Pharmaceuticals,Inc. | 2024-08-09 | HUMAN PRESCRIPTION DRUG LABEL | 2 |