Tamsulosin Hydrochloride
- Product NDC
- 55700-670
- 11-digit product format
- 557000670
- Labeler code
- 55700
- Product ID
- 55700-670_180060de-07ab-4cad-a02b-0b9631abbeb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA207405
- Marketing category
- ANDA
- Marketing start
- 2018-08-17
- 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
- 2022-12-31
- 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 |
|---|
| 55700-670-30 | 55700067030 | 30 CAPSULE in 1 BOTTLE (55700-670-30) | 30 capsule | 2018-08-17 | 0000-00-00 | No | No | Current |
| 55700-670-90 | 55700067090 | 90 CAPSULE in 1 BOTTLE (55700-670-90) | 90 capsule | 2018-08-17 | 0000-00-00 | No | No | Current |