Alfuzosin Hydrochloride 10 mg / 1 Tablet 100 Tablet, Extended Release
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 47335-0956-88 |
|---|---|
| Product NDC | 47335-0956 |
| Generic Drug Name | Alfuzosin Hydrochloride |
| Brand Name | Alfuzosin Hydrochloride |
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
| Strength | 10 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 100 Tablet, Extended Release |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88) |
| Active Ingredients | Alfuzosin Hydrochloride |
| Marketing Category | ANDA |
Unless explicitly stated in writing, no direct affiliation, sponsorship, or endorsement by individual product manufacturers with Premium Rx National, LLC should be implied. All brand names, trade names, and trademarks are the property of their respective owners and are presented solely for accurate product identification and informational reference.
NDC snapshot
Alfuzosin Hydrochloride 10 mg / 1 Tablet is tracked under NDC 47335-0956-88 and rolls up into product family 47335-0956. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 100 Tablet, Extended Release.
- Manufacturer: Sun Pharmaceutical Industries, Inc..
- Dosage form: Tablet.
- Family size: 5 indexed presentations.
Click a tag to refine the catalog view around this product reference.
Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Alternate presentations in this family
These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.
Alfuzosin Hydrochloride 10 mg / 1 Tablet 100 Tablet, Extended Release, NDC 47335-0956-88, is a Sun Pharmaceutical Industries, Inc. 10 mg / 1 tablet presentation packaged as 100 Tablet, Extended Release.
NDC search formats
- Canonical NDC 11: 47335-0956-88
- Digits-only NDC 11: 47335095688
- Possible 10-digit display format: 47335-956-88 (4733595688)
Helpful product links
- Search by brand name: Alfuzosin Hydrochloride
- NDC 11: 47335-0956-88
- Product family NDC: 47335-0956
- Other package sizes in this family: 1000 Tablet, Extended Release, 30 Tablet, Extended Release, 90 Tablet, Extended Release
- Compare related presentations: Alfuzosin Hydrochloride 10 mg / 1 Tablet 100 Tablet, Extended Release, Alfuzosin Hydrochloride 10 mg / 1 Tablet 1000 Tablet, Extended Release, Alfuzosin Hydrochloride 10 mg / 1 Tablet 30 Tablet, Extended Release, Alfuzosin Hydrochloride 10 mg / 1 Tablet 90 Tablet, Extended Release
- VA classification code: CV150
- VA classification code description: ALPHA BLOCKERS/RELATED
- CMOP ID: A1212
- VUID: 4017023