Package 63304-131-10
Brand: doxycycline
Generic: doxycyclinePackage Facts
Identity
Package NDC
63304-131-10
Digits Only
6330413110
Product NDC
63304-131
Description
1000 TABLET, FILM COATED in 1 BOTTLE (63304-131-10)
Marketing
Marketing Status
Brand
doxycycline
Generic
doxycycline
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fd417a50-69b5-40b4-89fd-58aea77ab547", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0363304173307"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["8224b9c5-5c4b-4dda-bc58-47b6604c2884"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (63304-131-01)", "package_ndc": "63304-131-01", "marketing_start_date": "20180806"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (63304-131-10)", "package_ndc": "63304-131-10", "marketing_start_date": "20180806"}], "brand_name": "Doxycycline", "product_id": "63304-131_fd417a50-69b5-40b4-89fd-58aea77ab547", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63304-131", "generic_name": "Doxycycline", "labeler_name": "Sun Pharmaceutical Industries Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "75 mg/1"}], "application_number": "ANDA065356", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20261231"}