Tamsulosin Hydrochloride
- Product NDC
- 16714-713
- 11-digit product format
- 167140713
- Labeler code
- 16714
- Product ID
- 16714-713_d4ffcb87-fd8f-430f-9d3a-26eb5b15ac95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA090931
- Marketing category
- ANDA
- Marketing start
- 2017-05-01
- 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 |
|---|
| 16714-713-01 | 16714071301 | 100 CAPSULE in 1 BOTTLE (16714-713-01) | 100 capsule | 2017-05-01 | 0000-00-00 | No | No | Current |
| 16714-713-02 | 16714071302 | 500 CAPSULE in 1 BOTTLE (16714-713-02) | 500 capsule | 2017-05-01 | 0000-00-00 | No | No | Current |