tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2052
Product ID 70518-2052_499bfb59-6626-9dd5-e063-6294a90abd9e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202433
Listing Expiration 2027-12-31
Marketing Start 2019-04-30

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182052
Hyphenated Format 70518-2052

Supplemental Identifiers

RxCUI
863669
UNII
11SV1951MR

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name tamsulosin hydrochloride (source: ndc)
Generic Name tamsulosin hydrochloride (source: ndc)
Application Number ANDA202433 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-0)
  • 30 CAPSULE in 1 BLISTER PACK (70518-2052-1)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-3)
  • 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-4)
source: ndc

Packages (4)

70518-2052-0 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-0) 70518-2052-1 30 CAPSULE in 1 BLISTER PACK (70518-2052-1) 70518-2052-3 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-3) 70518-2052-4 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-4)

Ingredients (1)

tamsulosin hydrochloride (.4 mg/1)

Linked Drug Pages (1)

Tamsulosin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "499bfb59-6626-9dd5-e063-6294a90abd9e", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["a608ddc8-fe42-484e-b61f-307c60151138"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-0)", "package_ndc": "70518-2052-0", "marketing_start_date": "20190430"}, {"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-2052-1)", "package_ndc": "70518-2052-1", "marketing_start_date": "20190610"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-3)", "package_ndc": "70518-2052-3", "marketing_start_date": "20250324"}, {"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (70518-2052-4)", "package_ndc": "70518-2052-4", "marketing_start_date": "20251010"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "70518-2052_499bfb59-6626-9dd5-e063-6294a90abd9e", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-2052", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA202433", "marketing_category": "ANDA", "marketing_start_date": "20190430", "listing_expiration_date": "20271231"}