Tamsulosin Hydrochloride
- Product NDC
- 55154-5359
- 11-digit product format
- 551545359
- Labeler code
- 55154
- Product ID
- 55154-5359_cfddaef8-758d-4d22-86bf-cdf63a181269
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA090408
- Marketing category
- ANDA
- Marketing start
- 2010-05-07
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record