clonazepam
Generic: clonazepam
Labeler: par health usa, llcDrug Facts
Product Profile
Brand Name
clonazepam
Generic Name
clonazepam
Labeler
par health usa, llc
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
clonazepam 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49884-310
Product ID
49884-310_8b72ac75-deb8-4acf-b411-9dd5d13dd51c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077171
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2005-08-05
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49884310
Hyphenated Format
49884-310
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
clonazepam (source: ndc)
Generic Name
clonazepam (source: ndc)
Application Number
ANDA077171 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-310-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8b72ac75-deb8-4acf-b411-9dd5d13dd51c", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0349884308025"], "unii": ["5PE9FDE8GB"], "rxcui": ["349194", "349195", "349196", "349197", "349198"], "spl_set_id": ["1aef0069-80ea-483d-ac70-c8d485462c5b"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-310-02)", "package_ndc": "49884-310-02", "marketing_start_date": "20050805"}], "brand_name": "Clonazepam", "product_id": "49884-310_8b72ac75-deb8-4acf-b411-9dd5d13dd51c", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "49884-310", "dea_schedule": "CIV", "generic_name": "clonazepam", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonazepam", "active_ingredients": [{"name": "CLONAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA077171", "marketing_category": "ANDA", "marketing_start_date": "20050805", "listing_expiration_date": "20261231"}