Nadolol
- Product NDC
- 60687-324
- 11-digit product format
- 606870324
- Labeler code
- 60687
- Product ID
- 60687-324_7017ec2a-396f-771d-e053-2991aa0ae9ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA203455
- Marketing category
- ANDA
- Marketing start
- 2017-04-19
- Marketing end
- 2019-03-31
- Substance
- NADOLOL
- Active strength
- 80 mg/1
- Pharmacologic classes
- Adrenergic beta
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record