doxycycline hyclate

Generic: doxycycline hyclate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7800
Product ID 50090-7800_198523f1-ce8e-42b5-adfe-6ebf3e78cdc3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062269
Listing Expiration 2026-12-31
Marketing Start 2025-03-07

Pharmacologic Class

Classes
tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907800
Hyphenated Format 50090-7800

Supplemental Identifiers

RxCUI
1650143
UNII
19XTS3T51U

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-7800-0)
source: ndc

Packages (1)

Ingredients (1)

doxycycline hyclate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "198523f1-ce8e-42b5-adfe-6ebf3e78cdc3", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["ca63aa91-519d-429f-adfc-a4ec45367294"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-7800-0)", "package_ndc": "50090-7800-0", "marketing_start_date": "20251125"}], "brand_name": "Doxycycline Hyclate", "product_id": "50090-7800_198523f1-ce8e-42b5-adfe-6ebf3e78cdc3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "50090-7800", "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": "20250307", "listing_expiration_date": "20261231"}