Nadolol
- Product NDC
- 0781-8004
- 11-digit product format
- 007818004
- Labeler code
- 0781
- Product ID
- 0781-8004_4ea4be37-c7b1-4035-85d1-4a7cb4e2be40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA074501
- Marketing category
- ANDA
- Marketing start
- 2008-10-01
- Marketing end
- 0000-00-00
- Substance
- NADOLOL
- Active strength
- 20 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 |
|---|
| 0781-8004-01 | 00781800401 | 100 TABLET in 1 BOTTLE (0781-8004-01) | 100 tablet | 2018-09-04 | 0000-00-00 | No | No | Current |
| 0781-8004-10 | 00781800410 | 1000 TABLET in 1 BOTTLE (0781-8004-10) | 1000 tablet | 2018-09-04 | 0000-00-00 | No | No | Current |
| 0781-8004-92 | 00781800492 | 90 TABLET in 1 BOTTLE (0781-8004-92) | 90 tablet | 2018-09-04 | 0000-00-00 | No | No | Current |