tamsulosin hydrochloride
- Product NDC
- 0904-6401
- 11-digit product format
- 009046401
- Labeler code
- 0904
- Product ID
- 0904-6401_4c7c59b5-fc0d-4bce-81b5-5b1ca798359b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078015
- Marketing category
- ANDA
- Marketing start
- 2015-01-05
- 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 |
|---|
| 0904-6401-61 | 00904640161 | 100 BLISTER PACK in 1 CARTON (0904-6401-61) > 1 CAPSULE in 1 BLISTER PACK | 100 blister pack | 2015-01-05 | 0000-00-00 | No | No | Current |
| 0904-6401-80 | 00904640180 | 1000 CAPSULE in 1 BOTTLE (0904-6401-80) | 1000 capsule | 2015-01-05 | 0000-00-00 | No | No | Current |
| 0904-6401-89 | 00904640189 | 90 CAPSULE in 1 BOTTLE (0904-6401-89) | 90 capsule | 2015-01-05 | 0000-00-00 | No | No | Current |