Pindolol
- Product NDC
- 70710-1064
- 11-digit product format
- 707101064
- Labeler code
- 70710
- Product ID
- 70710-1064_a480b773-72e8-460c-9541-89767ce97088
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pindolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA209866
- Marketing category
- ANDA
- Marketing start
- 2017-11-07
- Marketing end
- 0000-00-00
- Substance
- PINDOLOL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70710-1064-1 | 70710106401 | 100 TABLET in 1 BOTTLE (70710-1064-1) | 100 tablet | 2017-11-07 | 0000-00-00 | No | No | Current |