ethambutol hydrochloride

Generic: ethambutol hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ethambutol hydrochloride
Generic Name ethambutol hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ethambutol hydrochloride 400 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2966
Product ID 70518-2966_4aba550b-837b-4af9-e063-6394a90af074
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078939
Listing Expiration 2027-12-31
Marketing Start 2020-12-11

Pharmacologic Class

Classes
antimycobacterial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182966
Hyphenated Format 70518-2966

Supplemental Identifiers

RxCUI
995607
UNII
QE4VW5FO07

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 ethambutol hydrochloride (source: ndc)
Generic Name ethambutol hydrochloride (source: ndc)
Application Number ANDA078939 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-2966-0)
source: ndc

Packages (1)

70518-2966-0 30 TABLET in 1 BLISTER PACK (70518-2966-0)

Ingredients (1)

ethambutol hydrochloride (400 mg/1)

Linked Drug Pages (1)

Ethambutol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4aba550b-837b-4af9-e063-6394a90af074", "openfda": {"unii": ["QE4VW5FO07"], "rxcui": ["995607"], "spl_set_id": ["c12b3482-55f0-4324-bdcd-b129ca2dae73"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2966-0)", "package_ndc": "70518-2966-0", "marketing_start_date": "20201211"}], "brand_name": "Ethambutol Hydrochloride", "product_id": "70518-2966_4aba550b-837b-4af9-e063-6394a90af074", "dosage_form": "TABLET", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "70518-2966", "generic_name": "Ethambutol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethambutol Hydrochloride", "active_ingredients": [{"name": "ETHAMBUTOL HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA078939", "marketing_category": "ANDA", "marketing_start_date": "20201211", "listing_expiration_date": "20271231"}