venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler dr. reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 100 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-549
Product ID 55111-549_20a19933-a7c1-3739-c472-272204375d1e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078301
Listing Expiration 2026-12-31
Marketing Start 2008-06-16

Pharmacologic Class

Classes
norepinephrine uptake inhibitors [moa] serotonin uptake inhibitors [moa] serotonin and norepinephrine reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111549
Hyphenated Format 55111-549

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UNII
7D7RX5A8MO

Packaging Origin

Original Packager
true

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 venlafaxine hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA078301 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (55111-549-01)
  • 500 TABLET in 1 BOTTLE (55111-549-05)
  • 30 TABLET in 1 BOTTLE (55111-549-30)
  • 60 TABLET in 1 BOTTLE (55111-549-60)
  • 1 BLISTER PACK in 1 CARTON (55111-549-79) / 10 TABLET in 1 BLISTER PACK
  • 90 TABLET in 1 BOTTLE (55111-549-90)
source: ndc

Packages (6)

55111-549-01 100 TABLET in 1 BOTTLE (55111-549-01) 55111-549-05 500 TABLET in 1 BOTTLE (55111-549-05) 55111-549-30 30 TABLET in 1 BOTTLE (55111-549-30) 55111-549-60 60 TABLET in 1 BOTTLE (55111-549-60) 55111-549-79 1 BLISTER PACK in 1 CARTON (55111-549-79) / 10 TABLET in 1 BLISTER PACK 55111-549-90 90 TABLET in 1 BOTTLE (55111-549-90)

Ingredients (1)

venlafaxine hydrochloride (100 mg/1)

Linked Drug Pages (1)

Venlafaxine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "20a19933-a7c1-3739-c472-272204375d1e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["106d0d7b-925b-74e7-83cb-562144ce1f92"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-549-01)", "package_ndc": "55111-549-01", "marketing_start_date": "20080616"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-549-05)", "package_ndc": "55111-549-05", "marketing_start_date": "20080616"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-549-30)", "package_ndc": "55111-549-30", "marketing_start_date": "20080616"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55111-549-60)", "package_ndc": "55111-549-60", "marketing_start_date": "20080616"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (55111-549-79)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "55111-549-79", "marketing_start_date": "20080616"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55111-549-90)", "package_ndc": "55111-549-90", "marketing_start_date": "20080616"}], "brand_name": "Venlafaxine hydrochloride", "product_id": "55111-549_20a19933-a7c1-3739-c472-272204375d1e", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "55111-549", "generic_name": "Venlafaxine hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA078301", "marketing_category": "ANDA", "marketing_start_date": "20080616", "listing_expiration_date": "20261231"}