Nadolol
- Product NDC
- 31722-347
- 11-digit product format
- 317220347
- Labeler code
- 31722
- Product ID
- 31722-347_32deca47-c3a3-4b1e-80ad-22e4b1500282
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber, Pharmaceuticals Inc
- Application
- ANDA203455
- Marketing category
- ANDA
- Marketing start
- 2016-01-27
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-347 | NADOLOL TABLET [CAMBER, PHARMACEUTICALS INC] | 1 | Legacy NDC | 20160128_54b165a5-23ef-4c44-8971-02b757bba687.zip |