clindamycin phosphate and benzoyl peroxide

Generic: clindamycin and benzoyl peroxide gel

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clindamycin phosphate and benzoyl peroxide
Generic Name clindamycin and benzoyl peroxide gel
Labeler sun pharmaceutical industries, inc.
Dosage Form KIT
Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1381
Product ID 51672-1381_3962afa2-91b8-5444-e063-6394a90a3215
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208776
Listing Expiration 2026-12-31
Marketing Start 2018-05-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721381
Hyphenated Format 51672-1381

Supplemental Identifiers

RxCUI
308694 309333 358917

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 clindamycin phosphate and benzoyl peroxide (source: ndc)
Generic Name clindamycin and benzoyl peroxide gel (source: ndc)
Application Number ANDA208776 (source: ndc)

Resolved Composition

Strengths
  • 25 g
  • 20 g
  • 5 g
  • 35 g
  • 28 g
  • 7 g
  • 50 g
  • 40 g
  • 10 g
  • 1 %/5 %
source: label
Packaging
  • 1 KIT in 1 CARTON (51672-1381-2) * 5 g in 1 BOTTLE, PLASTIC (51672-1382-1) * 20 g in 1 JAR
source: ndc

Packages (1)

51672-1381-2 1 KIT in 1 CARTON (51672-1381-2) * 5 g in 1 BOTTLE, PLASTIC (51672-1382-1) * 20 g in 1 JAR

Ingredients (0)

No ingredient records.

Linked Drug Pages (4)

Clindamycin Phosphate and Benzoyl Peroxide ndc-match (0.9) Clindamycin Phosphate and Benzoyl Peroxide ndc-match (0.9) Clindamycin Phosphate and Benzoyl Peroxide ndc-match (0.9) Clindamycin Phosphate and Benzoyl Peroxide ndc-match (0.9)

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"}