doxycycline hyclate
Generic: doxycycline hyclate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
doxycycline hyclate
Generic Name
doxycycline hyclate
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
doxycycline hyclate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6134
Product ID
50090-6134_342f09d4-0649-4561-84d8-f667832ca920
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062269
Listing Expiration
2026-12-31
Marketing Start
2016-10-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906134
Hyphenated Format
50090-6134
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
doxycycline hyclate (source: ndc)
Generic Name
doxycycline hyclate (source: ndc)
Application Number
ANDA062269 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 2 TABLET, FILM COATED in 1 BOTTLE (50090-6134-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "342f09d4-0649-4561-84d8-f667832ca920", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["d70ae360-b2fb-44ba-a968-aba12e9c4469"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (50090-6134-6)", "package_ndc": "50090-6134-6", "marketing_start_date": "20221003"}], "brand_name": "Doxycycline Hyclate", "product_id": "50090-6134_342f09d4-0649-4561-84d8-f667832ca920", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "50090-6134", "generic_name": "Doxycycline Hyclate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_start_date": "20161001", "listing_expiration_date": "20261231"}