doxycycline

Generic: doxycycline

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

Drug Facts

Product Profile

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

doxycycline 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3809
Product ID 50090-3809_e226e0f6-37f7-4967-b524-e69835eeee6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209582
Listing Expiration 2026-12-31
Marketing Start 2018-01-11

Pharmacologic Class

Established (EPC)
tetracycline-class drug [epc]
Chemical Structure
tetracyclines [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903809
Hyphenated Format 50090-3809

Supplemental Identifiers

RxCUI
1650142
UNII
N12000U13O
NUI
N0000175882 N0000007948

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 (source: ndc)
Generic Name doxycycline (source: ndc)
Application Number ANDA209582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-3809-0)
source: ndc

Packages (1)

50090-3809-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-3809-0)

Ingredients (1)

doxycycline (100 mg/1)

Linked Drug Pages (1)

Doxycycline ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e226e0f6-37f7-4967-b524-e69835eeee6c", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1650142"], "spl_set_id": ["55873d3e-09c4-4726-acfe-5da581589575"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-3809-0)", "package_ndc": "50090-3809-0", "marketing_start_date": "20181112"}], "brand_name": "Doxycycline", "product_id": "50090-3809_e226e0f6-37f7-4967-b524-e69835eeee6c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "50090-3809", "generic_name": "Doxycycline", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA209582", "marketing_category": "ANDA", "marketing_start_date": "20180111", "listing_expiration_date": "20261231"}