Tolazamide
- Product NDC
- 55289-265
- 11-digit product format
- 552890265
- Labeler code
- 55289
- Product ID
- 55289-265_7b33fbac-3018-0b82-e053-2991aa0abc53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tolazamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA070259
- Marketing category
- ANDA
- Marketing start
- 2010-01-05
- Marketing end
- 0000-00-00
- Substance
- TOLAZAMIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record