Tamsulosin hydrochloride
- Product NDC
- 43063-264
- 11-digit product format
- 430630264
- Labeler code
- 43063
- Product ID
- 43063-264_d5f431b3-fe3d-7ddd-e053-2995a90ad815
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078801
- Marketing category
- ANDA
- Marketing start
- 2010-04-27
- Marketing end
- 0000-00-00
- Substance
- TAMSULOSIN HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-264-01 | 43063026401 | 100 CAPSULE in 1 BOTTLE, PLASTIC (43063-264-01) | 100 capsule | 2010-04-28 | 0000-00-00 | No | No | Current |
| 43063-264-30 | 43063026430 | 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-264-30) | 30 capsule | 2010-04-28 | 0000-00-00 | No | No | Current |
| 43063-264-90 | 43063026490 | 90 CAPSULE in 1 BOTTLE, PLASTIC (43063-264-90) | 90 capsule | 2010-04-28 | 0000-00-00 | No | No | Current |