Tamsulosin Hydrochloride
- Product NDC
- 60760-450
- 11-digit product format
- 607600450
- Labeler code
- 60760
- Product ID
- 60760-450_b96a08ae-b256-caca-e053-2995a90ab659
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA204645
- Marketing category
- ANDA
- Marketing start
- 2021-01-22
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-450 | TAMSULOSIN HYDROCHLORIDE CAPSULE [ST. MARY'S MEDICAL PARK PHARMACY] | 1 | Legacy NDC | 20210212_b969e0f3-1552-89d8-e053-2995a90acd7d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-450-90 | 60760045090 | 90 CAPSULE in 1 BOTTLE, PLASTIC (60760-450-90) | 90 capsule | 2021-01-22 | 0000-00-00 | No | No | Current |