Methazolamide
- Product NDC
- 0781-1072
- 11-digit product format
- 007811072
- Labeler code
- 0781
- Product ID
- 0781-1072_299cdbf2-a3f7-4912-b834-9880c8a86842
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methazolamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA040036
- Marketing category
- ANDA
- Marketing start
- 1993-06-30
- Marketing end
- 2021-09-30
- Substance
- METHAZOLAMIDE
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-1072-01 | 00781107201 | 100 TABLET in 1 BOTTLE (0781-1072-01) | 100 tablet | 1993-06-30 | 2021-03-31 | No | No | Current |