orphenadrine citrate
Generic: orphenadrine citrate
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
orphenadrine citrate
Generic Name
orphenadrine citrate
Labeler
actavis pharma, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
orphenadrine citrate 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0591-3222
Product ID
0591-3222_76bd2057-e1ac-4529-9663-f6139218eeab
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA084779
Listing Expiration
2026-12-31
Marketing Start
2010-07-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05913222
Hyphenated Format
0591-3222
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
orphenadrine citrate (source: ndc)
Generic Name
orphenadrine citrate (source: ndc)
Application Number
ANDA084779 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 10 AMPULE in 1 CARTON (0591-3222-47) / 2 mL in 1 AMPULE (0591-3222-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "76bd2057-e1ac-4529-9663-f6139218eeab", "openfda": {"unii": ["X0A40N8I4S"], "rxcui": ["994541"], "spl_set_id": ["aec8ad3a-f717-4e74-b7b9-19debdaad79a"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (0591-3222-47) / 2 mL in 1 AMPULE (0591-3222-02)", "package_ndc": "0591-3222-47", "marketing_start_date": "20100708"}], "brand_name": "Orphenadrine Citrate", "product_id": "0591-3222_76bd2057-e1ac-4529-9663-f6139218eeab", "dosage_form": "INJECTION", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0591-3222", "generic_name": "Orphenadrine Citrate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Orphenadrine Citrate", "active_ingredients": [{"name": "ORPHENADRINE CITRATE", "strength": "30 mg/mL"}], "application_number": "ANDA084779", "marketing_category": "ANDA", "marketing_start_date": "20100708", "listing_expiration_date": "20261231"}