AcetaZOLAMIDE
- Product NDC
- 67296-0801
- 11-digit product format
- 672960801
- Labeler code
- 67296
- Product ID
- 67296-0801_d5691a6a-4f57-4ddc-8ee7-0d2b56cf43ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- ANDA084840
- Marketing category
- ANDA
- Marketing start
- 1978-03-31
- Marketing end
- 0000-00-00
- Substance
- ACETAZOLAMIDE
- Active strength
- 250 1/1
- Pharmacologic classes
- Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 67296-0801-1 | AcetaZOLAMIDE | 56 in 1 BOTTLE | TABLET | 56 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0801 | ACETAZOLAMIDE TABLET [REDPHARM DRUG INC.] | 1 | Legacy NDC, 1 package rows | 20110808_6972d9c1-36ec-4246-bf7b-13206d5952c3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0801-1 | 67296080101 | 56 in 1 BOTTLE | Historical |