Nadolol
- Product NDC
- 51079-812
- 11-digit product format
- 510790812
- Labeler code
- 51079
- Product ID
- 51079-812_d34804f5-bcfc-3c6e-e053-2a95a90a770c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA074172
- Marketing category
- ANDA
- Marketing start
- 1994-07-12
- Marketing end
- 2023-08-31
- Substance
- NADOLOL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- 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 |
|---|
| 51079-812-20 | 51079081220 | 100 BLISTER PACK in 1 CARTON (51079-812-20) > 1 TABLET in 1 BLISTER PACK (51079-812-01) | 100 blister pack | 1994-07-12 | 0000-00-00 | No | No | Current |