doxycycline

Generic: doxycycline hyclate

Labeler: acella pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline hyclate
Labeler acella pharmaceuticals, llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Acella Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 42192-501
Product ID 42192-501_3b12eb84-4431-551b-e063-6294a90acd6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210664
Listing Expiration 2026-12-31
Marketing Start 2020-08-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42192501
Hyphenated Format 42192-501

Supplemental Identifiers

RxCUI
1650143
UPC
0342192501058
UNII
19XTS3T51U

Packaging Origin

Original Packager
true

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 hyclate (source: ndc)
Application Number ANDA210664 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 500 TABLET, COATED in 1 BOTTLE (42192-501-05)
  • 50 TABLET, COATED in 1 BOTTLE (42192-501-50)
source: ndc

Packages (2)

42192-501-05 500 TABLET, COATED in 1 BOTTLE (42192-501-05) 42192-501-50 50 TABLET, COATED in 1 BOTTLE (42192-501-50)

Ingredients (1)

doxycycline hyclate (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": "3b12eb84-4431-551b-e063-6294a90acd6c", "openfda": {"upc": ["0342192501058"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["3fb9f5ad-90a2-4858-bc34-f800d8b2fa90"], "manufacturer_name": ["Acella Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (42192-501-05)", "package_ndc": "42192-501-05", "marketing_start_date": "20200821"}, {"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (42192-501-50)", "package_ndc": "42192-501-50", "marketing_start_date": "20200821"}], "brand_name": "Doxycycline", "product_id": "42192-501_3b12eb84-4431-551b-e063-6294a90acd6c", "dosage_form": "TABLET, COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "42192-501", "generic_name": "Doxycycline hyclate", "labeler_name": "Acella Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA210664", "marketing_category": "ANDA", "marketing_start_date": "20200821", "listing_expiration_date": "20261231"}