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NDC 65862-0249-01 Alfuzosin Hydrochloride 10 mg/1 Details
Alfuzosin Hydrochloride 10 mg/1
Alfuzosin Hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is ALFUZOSIN HYDROCHLORIDE.
MedlinePlus Drug Summary
Alfuzosin is used in men to treat symptoms of an enlarged prostate (benign prostatic hyperplasia or BPH), which include difficulty urinating (hesitation, dribbling, weak stream, and incomplete bladder emptying), painful urination, and urinary frequency and urgency. Alfuzosin is in a class of medications called alpha blockers. It works by relaxing the muscles in the prostate and bladder to allow urine to flow more easily.
Related Packages: 65862-0249-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Alfuzosin
Product Information
| NDC | 65862-0249 |
|---|---|
| Product ID | 65862-249_d8c832c1-9455-4647-822a-ee4f35ba0560 |
| Associated GPIs | 56852010107530 |
| GCN Sequence Number | 045052 |
| GCN Sequence Number Description | alfuzosin HCl TAB ER 24H 10 MG ORAL |
| HIC3 | Q9B |
| HIC3 Description | BENIGN PROSTATIC HYPERTROPHY/MICTURITION AGENTS |
| GCN | 92024 |
| HICL Sequence Number | 010802 |
| HICL Sequence Number Description | ALFUZOSIN HCL |
| Brand/Generic | Generic |
| Proprietary Name | Alfuzosin Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Alfuzosin Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | ALFUZOSIN HYDROCHLORIDE |
| Labeler Name | Aurobindo Pharma Limited |
| Pharmaceutical Class | Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA079060 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 65862-0249-01 (65862024901)
| NDC Package Code | 65862-249-01 |
|---|---|
| Billing NDC | 65862024901 |
| Package | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01) |
| Marketing Start Date | 2012-08-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |