Pindolol
- Product NDC
- 29033-029
- 11-digit product format
- 290330029
- Labeler code
- 29033
- Product ID
- 29033-029_b00152ed-f667-4169-9082-e15730302669
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pindolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Nostrum Laboratories, Inc.
- Application
- ANDA205415
- Marketing category
- ANDA
- Marketing start
- 2016-02-01
- 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
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 29033-029-01 | Pindolol | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29033-029 | PINDOLOL TABLET [NOSTRUM LABORATORIES, INC.] | 3 | Legacy NDC, 1 package rows | 20181218_0648878e-ba6e-4901-948e-f6dcff9fe082.zip |
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 |
|---|
| 29033-029-01 | 29033002901 | 100 TABLET in 1 BOTTLE (29033-029-01) | 100 tablet | 2016-02-01 | 0000-00-00 | No | No | Current |