doxycycline hyclate

Generic: doxycycline hyclate

Labeler: chartwell governmental & specialty rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler chartwell governmental & specialty rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 50 mg/1

Manufacturer
Chartwell Governmental & Specialty RX, LLC

Identifiers & Regulatory

Product NDC 68999-625
Product ID 68999-625_40076faf-09c3-f4ab-e063-6394a90ab3c1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062505
Listing Expiration 2026-12-31
Marketing Start 2021-07-21

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 68999625
Hyphenated Format 68999-625

Supplemental Identifiers

RxCUI
1649405 1649988 1650030 1650143 1652674
UPC
0368999626404 0368999626282 0368999625605 0368999985501 0368999984504 0368999417460 0368999626305 0368999626060 0368999626312 0368999626503
UNII
19XTS3T51U N12000U13O
NUI
N0000175882 N0000007948

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 hyclate (source: ndc)
Generic Name doxycycline hyclate (source: ndc)
Application Number ANDA062505 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (68999-625-60)
source: ndc

Packages (1)

68999-625-60 60 TABLET, FILM COATED in 1 BOTTLE (68999-625-60)

Ingredients (1)

doxycycline hyclate (50 mg/1)

Linked Drug Pages (1)

doxycycline, Doxycycline Hyclate, doxycycline hyclate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40076faf-09c3-f4ab-e063-6394a90ab3c1", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0368999626404", "0368999626282", "0368999625605", "0368999985501", "0368999984504", "0368999417460", "0368999626305", "0368999626060", "0368999626312", "0368999626503"], "unii": ["19XTS3T51U", "N12000U13O"], "rxcui": ["1649405", "1649988", "1650030", "1650143", "1652674"], "spl_set_id": ["b8486639-7eb9-4610-9cd4-0e922045d592"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68999-625-60)", "package_ndc": "68999-625-60", "marketing_start_date": "20210901"}], "brand_name": "Doxycycline Hyclate", "product_id": "68999-625_40076faf-09c3-f4ab-e063-6394a90ab3c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68999-625", "generic_name": "Doxycycline Hyclate", "labeler_name": "Chartwell Governmental & Specialty RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "50 mg/1"}], "application_number": "ANDA062505", "marketing_category": "ANDA", "marketing_start_date": "20210721", "listing_expiration_date": "20261231"}