Tamsulosin Hydrochloride
- Product NDC
- 68071-4585
- 11-digit product format
- 680714585
- Labeler code
- 68071
- Product ID
- 68071-4585_776b3591-50b4-1999-e053-2991aa0a42bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record