Tamsulosin Hydrochloride
- Product NDC
- 0378-2500
- 11-digit product format
- 003782500
- Labeler code
- 0378
- Product ID
- 0378-2500_d71e940c-17b7-46a0-b95d-e484594aa4b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA090408
- Marketing category
- ANDA
- Marketing start
- 2010-04-27
- Marketing end
- 2019-11-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record