tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-688
Product ID 71205-688_58cba3d8-bb57-4e64-a191-dc050904c896
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202433
Listing Expiration 2026-12-31
Marketing Start 2013-04-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205688
Hyphenated Format 71205-688

Supplemental Identifiers

RxCUI
863669
UPC
0371205688141
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
  • 7 CAPSULE in 1 BOTTLE (71205-688-07)
  • 14 CAPSULE in 1 BOTTLE (71205-688-14)
  • 30 CAPSULE in 1 BOTTLE (71205-688-30)
  • 60 CAPSULE in 1 BOTTLE (71205-688-60)
  • 90 CAPSULE in 1 BOTTLE (71205-688-90)
source: ndc

Packages (5)

71205-688-07 7 CAPSULE in 1 BOTTLE (71205-688-07) 71205-688-14 14 CAPSULE in 1 BOTTLE (71205-688-14) 71205-688-30 30 CAPSULE in 1 BOTTLE (71205-688-30) 71205-688-60 60 CAPSULE in 1 BOTTLE (71205-688-60) 71205-688-90 90 CAPSULE in 1 BOTTLE (71205-688-90)

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": "58cba3d8-bb57-4e64-a191-dc050904c896", "openfda": {"upc": ["0371205688141"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["58cba3d8-bb57-4e64-a191-dc050904c896"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "7 CAPSULE in 1 BOTTLE (71205-688-07)", "package_ndc": "71205-688-07", "marketing_start_date": "20220822"}, {"sample": false, "description": "14 CAPSULE in 1 BOTTLE (71205-688-14)", "package_ndc": "71205-688-14", "marketing_start_date": "20220822"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-688-30)", "package_ndc": "71205-688-30", "marketing_start_date": "20220822"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-688-60)", "package_ndc": "71205-688-60", "marketing_start_date": "20220822"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-688-90)", "package_ndc": "71205-688-90", "marketing_start_date": "20220822"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "71205-688_58cba3d8-bb57-4e64-a191-dc050904c896", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71205-688", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Proficient Rx LP", "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": "20130430", "listing_expiration_date": "20261231"}