Tamsulosin Hydrochloride
- Product NDC
- 10370-169
- 11-digit product format
- 103700169
- Labeler code
- 10370
- Product ID
- 10370-169_2a77502d-c2bf-4f3d-81c0-7f227ef4bfa1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA202010
- Marketing category
- ANDA
- Marketing start
- 2013-03-19
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10370-169-01 | 10370016901 | 100 CAPSULE in 1 BOTTLE (10370-169-01) | 100 capsule | 2013-03-19 | 0000-00-00 | No | No | Current |
| 10370-169-05 | 10370016905 | 500 CAPSULE in 1 BOTTLE (10370-169-05) | 500 capsule | 2013-03-19 | 0000-00-00 | No | No | Current |