acetaZOLAMIDE
- Product NDC
- 50090-7536
- 11-digit product format
- 500907536
- Labeler code
- 50090
- Product ID
- 50090-7536_0c0d69e8-f78e-4286-ad4a-77e3719e16ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetaZOLAMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211069
- Marketing category
- ANDA
- Marketing start
- 2023-07-15
- Substance
- ACETAZOLAMIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- acetaZOLAMIDE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAZOLAMIDE | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O3FX965V0I |
| Rxcui | 197304 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7536-0 | acetaZOLAMIDE | 12 in 1 BOTTLE | TABLET | 12 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7536 | ACETAZOLAMIDE TABLET [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 1 package rows | 20250417_b339843f-0324-4996-88a0-0619fd6f867b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7536-0 | 50090753600 | 12 TABLET in 1 BOTTLE (50090-7536-0) | 12 tablet | 2025-04-09 | No | No | Historical |