Package 51672-1381-2
Brand: clindamycin phosphate and benzoyl peroxide
Generic: clindamycin and benzoyl peroxide gelPackage Facts
Identity
Package NDC
51672-1381-2
Digits Only
5167213812
Product NDC
51672-1381
Description
1 KIT in 1 CARTON (51672-1381-2) * 5 g in 1 BOTTLE, PLASTIC (51672-1382-1) * 20 g in 1 JAR
Marketing
Marketing Status
Brand
clindamycin phosphate and benzoyl peroxide
Generic
clindamycin and benzoyl peroxide gel
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "3962afa2-91b8-5444-e063-6394a90a3215", "openfda": {"rxcui": ["308694", "309333", "358917"], "spl_set_id": ["3b151c49-d44c-4a24-b7ff-329797a2cda3"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (51672-1381-2) * 5 g in 1 BOTTLE, PLASTIC (51672-1382-1) * 20 g in 1 JAR", "package_ndc": "51672-1381-2", "marketing_start_date": "20180525"}], "brand_name": "Clindamycin Phosphate and Benzoyl Peroxide", "product_id": "51672-1381_3962afa2-91b8-5444-e063-6394a90a3215", "dosage_form": "KIT", "product_ndc": "51672-1381", "generic_name": "Clindamycin and Benzoyl Peroxide Gel", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clindamycin Phosphate and Benzoyl Peroxide", "application_number": "ANDA208776", "marketing_category": "ANDA", "marketing_start_date": "20180525", "listing_expiration_date": "20261231"}