doxycycline

Generic: doxycycline

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline
Labeler zydus pharmaceuticals usa inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline 150 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1124
Product ID 70710-1124_24db9fe2-5c05-42d0-b113-307484699e9a
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 707101124
Hyphenated Format 70710-1124

Supplemental Identifiers

RxCUI
1649429 1650142 1650444 1652673
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 ANDA209582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (70710-1124-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)
source: ndc

Packages (2)

70710-1124-1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1124-1) 70710-1124-3 30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)

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": "24db9fe2-5c05-42d0-b113-307484699e9a", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["bc321932-b600-4659-a499-1853991b4ab9"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1124-1)", "package_ndc": "70710-1124-1", "marketing_start_date": "20180111"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)", "package_ndc": "70710-1124-3", "marketing_start_date": "20180111"}], "brand_name": "Doxycycline", "product_id": "70710-1124_24db9fe2-5c05-42d0-b113-307484699e9a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70710-1124", "generic_name": "Doxycycline", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "150 mg/1"}], "application_number": "ANDA209582", "marketing_category": "ANDA", "marketing_start_date": "20180111", "listing_expiration_date": "20261231"}