Tamsulosin Hydrochloride
- Product NDC
- 50436-0119
- 11-digit product format
- 504360119
- Labeler code
- 50436
- Product ID
- 50436-0119_9f7a82cb-cb37-48c7-bed5-993fe0c94573
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA090931
- Marketing category
- ANDA
- Marketing start
- 2010-07-15
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record