Nadolol
- Product NDC
- 0904-7070
- 11-digit product format
- 009047070
- Labeler code
- 0904
- Product ID
- 0904-7070_fc852b15-5479-4623-a911-95583bcb0089
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA203455
- Marketing category
- ANDA
- Marketing start
- 2016-02-23
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7070 | NADOLOL TABLET [MAJOR PHARMACEUTICALS] | 6 | Legacy NDC | 20241215_58ae7b7e-fa22-486b-9fa3-cfb31d81c637.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7070-07 | 00904707007 | 30 BLISTER PACK in 1 CARTON (0904-7070-07) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2016-02-23 | 0000-00-00 | No | No | Current |
| 0904-7070-61 | 00904707061 | 100 BLISTER PACK in 1 CARTON (0904-7070-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2016-02-23 | 0000-00-00 | No | No | Current |