doxycycline hyclate

Generic: doxycycline hyclate

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler redpharm drug
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2075
Product ID 67296-2075_2c641265-66df-dc3f-e063-6394a90a5a55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211343
Listing Expiration 2026-12-31
Marketing Start 2019-10-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672962075
Hyphenated Format 67296-2075

Supplemental Identifiers

RxCUI
1650143
UPC
0327808234018 0327808234025
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 ANDA211343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (67296-2075-2)
source: ndc

Packages (1)

Ingredients (1)

doxycycline hyclate (100 mg/1)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c641265-66df-dc3f-e063-6394a90a5a55", "openfda": {"upc": ["0327808234018", "0327808234025"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["0b251a58-30d8-dfec-e063-6294a90a3b45"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (67296-2075-2)", "package_ndc": "67296-2075-2", "marketing_start_date": "20220214"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "67296-2075_2c641265-66df-dc3f-e063-6394a90a5a55", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "67296-2075", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA211343", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}