doxycycline
Generic: doxycycline
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
doxycycline
Generic Name
doxycycline
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
doxycycline 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-491
Product ID
72789-491_30278a66-373d-fba7-e063-6394a90a5ecf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205115
Listing Expiration
2026-12-31
Marketing Start
2016-03-14
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789491
Hyphenated Format
72789-491
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA205115 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 14 CAPSULE in 1 BOTTLE, PLASTIC (72789-491-14)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30278a66-373d-fba7-e063-6394a90a5ecf", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0372789491141"], "unii": ["N12000U13O"], "rxcui": ["1649990"], "spl_set_id": ["dedebcb4-3c3f-4487-a488-36af12640c92"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (72789-491-14)", "package_ndc": "72789-491-14", "marketing_start_date": "20250312"}], "brand_name": "doxycycline", "product_id": "72789-491_30278a66-373d-fba7-e063-6394a90a5ecf", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72789-491", "generic_name": "doxycycline", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA205115", "marketing_category": "ANDA", "marketing_start_date": "20160314", "listing_expiration_date": "20261231"}