Tamsulosin Hydrochloride
- Product NDC
- 68788-9421
- 11-digit product format
- 687889421
- Labeler code
- 68788
- Product ID
- 68788-9421_ab032f62-7476-41ea-8629-fb7702e13f57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA090931
- Marketing category
- ANDA
- Marketing start
- 2014-05-08
- 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