Pindolol
- Product NDC
- 68151-3005
- 11-digit product format
- 681513005
- Labeler code
- 68151
- Product ID
- 68151-3005_8744e0e2-01ec-4349-bf13-314950fdd04a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pindolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA074019
- Marketing category
- ANDA
- Marketing start
- 1992-09-03
- Marketing end
- 0000-00-00
- Substance
- PINDOLOL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-3005-0 | Pindolol | 1 in 1 PACKAGE | TABLET | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-3005 | PINDOLOL TABLET [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160806_a369da5a-ee4a-487f-9891-47955e565fb2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-3005-0 | 68151300500 | 1 in 1 PACKAGE | Historical |