tamsulosin hydrochloride
- Product NDC
- 55154-7649
- 11-digit product format
- 551547649
- Labeler code
- 55154
- Product ID
- 55154-7649_5b43d772-e6bf-4e0b-9e26-393cf0dd6881
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA078015
- Marketing category
- ANDA
- Marketing start
- 2015-01-05
- 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 |
|---|
| 55154-7649-0 | 55154764900 | 10 BLISTER PACK in 1 BAG (55154-7649-0) > 1 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2015-01-05 | 0000-00-00 | No | No | Current |