venlafaxine hydrochloride
Generic: venlafaxine hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
venlafaxine hydrochloride
Generic Name
venlafaxine hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
venlafaxine hydrochloride 37.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8682
Product ID
68788-8682_96b77279-4664-43cc-ae1e-dd893b00c6d2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214654
Listing Expiration
2026-12-31
Marketing Start
2024-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888682
Hyphenated Format
68788-8682
Supplemental Identifiers
RxCUI
UNII
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
ANDA214654 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 37.5 mg/1
Packaging
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-1)
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-3)
- 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-6)
- 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-8)
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-9)
Packages (5)
68788-8682-1
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-1)
68788-8682-3
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-3)
68788-8682-6
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-6)
68788-8682-8
120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-8)
68788-8682-9
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "96b77279-4664-43cc-ae1e-dd893b00c6d2", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["92b3f73d-d6ca-4d7d-9035-5700f527cb85"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-1)", "package_ndc": "68788-8682-1", "marketing_start_date": "20240601"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-3)", "package_ndc": "68788-8682-3", "marketing_start_date": "20240601"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-6)", "package_ndc": "68788-8682-6", "marketing_start_date": "20240601"}, {"sample": false, "description": "120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-8)", "package_ndc": "68788-8682-8", "marketing_start_date": "20240601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-9)", "package_ndc": "68788-8682-9", "marketing_start_date": "20240601"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8682_96b77279-4664-43cc-ae1e-dd893b00c6d2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8682", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}