Tamsulosin Hydrochloride
- Product NDC
- 55700-200
- 11-digit product format
- 557000200
- Labeler code
- 55700
- Product ID
- 55700-200_0cea8707-47ed-44f7-916f-1ee4910bb3f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202433
- Marketing category
- ANDA
- Marketing start
- 2013-04-30
- 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