Nadolol
- Product NDC
- 23155-732
- 11-digit product format
- 231550732
- Labeler code
- 23155
- Product ID
- 23155-732_7ce5fe0a-cf3d-4ef6-892c-b737f87c33e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA074255
- Marketing category
- ANDA
- Marketing start
- 2020-07-10
- Marketing end
- 0000-00-00
- Substance
- NADOLOL
- Active strength
- 80 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-732-01 | 23155073201 | 100 TABLET in 1 BOTTLE (23155-732-01) | 100 tablet | 2020-07-10 | 0000-00-00 | No | No | Current |
| 23155-732-09 | 23155073209 | 90 TABLET in 1 BOTTLE (23155-732-09) | 90 tablet | 2021-02-26 | 0000-00-00 | No | No | Current |
| 23155-732-10 | 23155073210 | 1000 TABLET in 1 BOTTLE (23155-732-10) | 1000 tablet | 2021-02-26 | 0000-00-00 | No | No | Current |