Pindolol
- Product NDC
- 70771-1134
- 11-digit product format
- 707711134
- Labeler code
- 70771
- Product ID
- 70771-1134_ec315429-b8ae-41bd-a745-bf607ec834d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pindolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA209866
- Marketing category
- ANDA
- Marketing start
- 2017-11-07
- Marketing end
- 0000-00-00
- Substance
- PINDOLOL
- Active strength
- 5 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 |
|---|
| 70771-1134-1 | 70771113401 | 100 TABLET in 1 BOTTLE (70771-1134-1) | 100 tablet | 2017-11-07 | 0000-00-00 | No | No | Current |