venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: dr.reddy's laboratories ltd.
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 ltd.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
Dr.Reddy's Laboratories Ltd.

Identifiers & Regulatory

Product NDC 55111-455
Product ID 55111-455_a0b75dbc-2382-70bc-7bd9-c6ef3ee4ed3e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078421
Listing Expiration 2026-12-31
Marketing Start 2011-06-01

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 55111455
Hyphenated Format 55111-455

Supplemental Identifiers

RxCUI
313581 313583 313585
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 ANDA078421 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-01)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-05)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-30)
  • 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-60)
  • 10 BLISTER PACK in 1 CARTON (55111-455-78) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (55111-455-79)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-90)
source: ndc

Packages (6)

55111-455-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-01) 55111-455-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-05) 55111-455-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-30) 55111-455-60 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-60) 55111-455-78 10 BLISTER PACK in 1 CARTON (55111-455-78) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (55111-455-79) 55111-455-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-90)

Ingredients (1)

venlafaxine hydrochloride (150 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": "a0b75dbc-2382-70bc-7bd9-c6ef3ee4ed3e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["7027be98-61d6-a986-c9df-60ceef5f7ff0"], "manufacturer_name": ["Dr.Reddy's Laboratories Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-01)", "package_ndc": "55111-455-01", "marketing_start_date": "20110601"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-05)", "package_ndc": "55111-455-05", "marketing_start_date": "20110601"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-30)", "package_ndc": "55111-455-30", "marketing_start_date": "20110601"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-60)", "package_ndc": "55111-455-60", "marketing_start_date": "20110601"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-455-78)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (55111-455-79)", "package_ndc": "55111-455-78", "marketing_start_date": "20110601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-90)", "package_ndc": "55111-455-90", "marketing_start_date": "20110601"}], "brand_name": "venlafaxine hydrochloride", "product_id": "55111-455_a0b75dbc-2382-70bc-7bd9-c6ef3ee4ed3e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "55111-455", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Dr.Reddy's Laboratories Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA078421", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}