Tamsulosin hydrochloride
- Product NDC
- 63629-6807
- 11-digit product format
- 636296807
- Labeler code
- 63629
- Product ID
- 63629-6807_113c2dcd-4c6b-4609-a1fc-88e2cd2527ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6807-1 | 63629680701 | 30 CAPSULE in 1 BOTTLE (63629-6807-1) | 30 capsule | 2015-10-12 | 0000-00-00 | No | No | Current |
| 63629-6807-2 | 63629680702 | 60 CAPSULE in 1 BOTTLE (63629-6807-2) | 60 capsule | 2015-10-12 | 0000-00-00 | No | No | Current |