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NDC 70934-0092-90 Tamsulosin Hydrochloride 0.4 mg/1 Details
Tamsulosin Hydrochloride 0.4 mg/1
Tamsulosin Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is TAMSULOSIN HYDROCHLORIDE.
Product Information
| NDC | 70934-0092 |
|---|---|
| Product ID | 70934-092_d8a295e4-63ea-984a-e053-2995a90a216f |
| Associated GPIs | 56852070100110 |
| GCN Sequence Number | 027546 |
| GCN Sequence Number Description | tamsulosin HCl CAPSULE 0.4 MG ORAL |
| HIC3 | Q9B |
| HIC3 Description | BENIGN PROSTATIC HYPERTROPHY/MICTURITION AGENTS |
| GCN | 48191 |
| HICL Sequence Number | 013864 |
| HICL Sequence Number Description | TAMSULOSIN HCL |
| Brand/Generic | Generic |
| Proprietary Name | Tamsulosin Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Tamsulosin Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 0.4 |
| Active Ingredient Units | mg/1 |
| Substance Name | TAMSULOSIN HYDROCHLORIDE |
| Labeler Name | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
| Pharmaceutical Class | Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA202433 |
| Listing Certified Through | n/a |
Package
NDC 70934-0092-90 (70934009290)
| NDC Package Code | 70934-092-90 |
|---|---|
| Billing NDC | 70934009290 |
| Package | 90 CAPSULE in 1 BOTTLE, PLASTIC (70934-092-90) |
| Marketing Start Date | 2020-06-22 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |