Corgard
- Product NDC
- 78670-100
- 11-digit product format
- 786700100
- Labeler code
- 78670
- Product ID
- 78670-100_88f9bb1e-0b4b-4d58-89aa-d1d88b5f7f5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- USWM, LLC
- Application
- NDA018063
- Marketing category
- NDA
- Marketing start
- 2022-02-01
- 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 |
|---|
| 78670-100-01 | 78670010001 | 100 TABLET in 1 BOTTLE (78670-100-01) | 100 tablet | 2021-11-18 | 0000-00-00 | No | No | Current |