tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler american health packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-299
Product ID 68084-299_38cbc0fa-ca6b-0e39-e063-6394a90abb97
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078225
Listing Expiration 2026-12-31
Marketing Start 2014-01-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68084299
Hyphenated Format 68084-299

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 ANDA078225 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-299-01) / 1 CAPSULE in 1 BLISTER PACK (68084-299-11)
  • 50 BLISTER PACK in 1 CARTON (68084-299-65) / 1 CAPSULE in 1 BLISTER PACK (68084-299-11)
source: ndc

Packages (2)

68084-299-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-299-01) / 1 CAPSULE in 1 BLISTER PACK (68084-299-11) 68084-299-65 50 BLISTER PACK in 1 CARTON (68084-299-65) / 1 CAPSULE in 1 BLISTER PACK (68084-299-11)

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": "38cbc0fa-ca6b-0e39-e063-6394a90abb97", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["8150a710-aee5-4841-ae1b-7d2e61281a8f"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-299-01)  / 1 CAPSULE in 1 BLISTER PACK (68084-299-11)", "package_ndc": "68084-299-01", "marketing_start_date": "20140117"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (68084-299-65)  / 1 CAPSULE in 1 BLISTER PACK (68084-299-11)", "package_ndc": "68084-299-65", "marketing_start_date": "20250701"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "68084-299_38cbc0fa-ca6b-0e39-e063-6394a90abb97", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68084-299", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA078225", "marketing_category": "ANDA", "marketing_start_date": "20140117", "listing_expiration_date": "20261231"}