AcetaZOLAMIDE
- Product NDC
- 50090-3003
- 11-digit product format
- 500903003
- Labeler code
- 50090
- Product ID
- 50090-3003_f47a5e0d-3ae0-413e-9be2-eeab28b40b23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA084840
- Marketing category
- ANDA
- Marketing start
- 1978-03-31
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 50090-3003-0 | AcetaZOLAMIDE | 12 in 1 BOTTLE | TABLET | 12 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3003 | ACETAZOLAMIDE TABLET [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC, 1 package rows | 20210417_abea2572-d579-42d3-97c8-1ebacefa9122.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3003-0 | 50090300300 | 12 TABLET in 1 BOTTLE (50090-3003-0) | 12 tablet | 2017-05-04 | 0000-00-00 | No | No | Current |