doxycycline

Generic: doxycycline

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline
Labeler lannett company, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline 150 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-1537
Product ID 0527-1537_dc960a6c-1b09-4049-a1e9-0109576b1d30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065285
Listing Expiration 2026-12-31
Marketing Start 2008-08-25

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 05271537
Hyphenated Format 0527-1537

Supplemental Identifiers

RxCUI
1649429 1650142 1650444 1652673
UPC
0305271537300 0305271535016
UNII
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 (source: ndc)
Generic Name doxycycline (source: ndc)
Application Number ANDA065285 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-01)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-30)
source: ndc

Packages (2)

0527-1537-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-01) 0527-1537-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-30)

Ingredients (1)

doxycycline (150 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": "dc960a6c-1b09-4049-a1e9-0109576b1d30", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0305271537300", "0305271535016"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["4999bbd9-44ed-4749-9730-be2337bdf490"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-01)", "package_ndc": "0527-1537-01", "marketing_start_date": "20080825"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-30)", "package_ndc": "0527-1537-30", "marketing_start_date": "20080825"}], "brand_name": "Doxycycline", "product_id": "0527-1537_dc960a6c-1b09-4049-a1e9-0109576b1d30", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0527-1537", "generic_name": "Doxycycline", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "150 mg/1"}], "application_number": "ANDA065285", "marketing_category": "ANDA", "marketing_start_date": "20080825", "listing_expiration_date": "20261231"}