clindamycin hydrochloride

Generic: clindamycin hydrochloride

Labeler: verityrx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clindamycin hydrochloride
Generic Name clindamycin hydrochloride
Labeler verityrx, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

clindamycin hydrochloride 300 mg/1

Manufacturer
VERITYRX, LLC

Identifiers & Regulatory

Product NDC 83939-0019
Product ID 83939-0019_4279fa58-a34a-daf6-e063-6294a90afbbe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065442
Listing Expiration 2026-12-31
Marketing Start 2009-08-26

Pharmacologic Class

Classes
decreased sebaceous gland activity [pe] lincosamide antibacterial [epc] lincosamides [cs] neuromuscular blockade [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 839390019
Hyphenated Format 83939-0019

Supplemental Identifiers

RxCUI
284215
UNII
T20OQ1YN1W

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 hydrochloride (source: ndc)
Generic Name clindamycin hydrochloride (source: ndc)
Application Number ANDA065442 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 1 CAPSULE in 1 POUCH (83939-0019-1)
  • 50 POUCH in 1 BOX, UNIT-DOSE (83939-0019-2) / 1 CAPSULE in 1 POUCH
  • 100 POUCH in 1 BOX, UNIT-DOSE (83939-0019-3) / 1 CAPSULE in 1 POUCH
source: ndc

Packages (3)

83939-0019-1 1 CAPSULE in 1 POUCH (83939-0019-1) 83939-0019-2 50 POUCH in 1 BOX, UNIT-DOSE (83939-0019-2) / 1 CAPSULE in 1 POUCH 83939-0019-3 100 POUCH in 1 BOX, UNIT-DOSE (83939-0019-3) / 1 CAPSULE in 1 POUCH

Ingredients (1)

clindamycin hydrochloride (300 mg/1)

Linked Drug Pages (1)

Clindamycin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4279fa58-a34a-daf6-e063-6294a90afbbe", "openfda": {"unii": ["T20OQ1YN1W"], "rxcui": ["284215"], "spl_set_id": ["427a0138-c2dd-cf0b-e063-6394a90af407"], "manufacturer_name": ["VERITYRX, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 CAPSULE in 1 POUCH (83939-0019-1)", "package_ndc": "83939-0019-1", "marketing_start_date": "20251103"}, {"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (83939-0019-2)  / 1 CAPSULE in 1 POUCH", "package_ndc": "83939-0019-2", "marketing_start_date": "20251103"}, {"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (83939-0019-3)  / 1 CAPSULE in 1 POUCH", "package_ndc": "83939-0019-3", "marketing_start_date": "20251103"}], "brand_name": "Clindamycin Hydrochloride", "product_id": "83939-0019_4279fa58-a34a-daf6-e063-6294a90afbbe", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Sebaceous Gland Activity [PE]", "Lincosamide Antibacterial [EPC]", "Lincosamides [CS]", "Neuromuscular Blockade [PE]"], "product_ndc": "83939-0019", "generic_name": "Clindamycin Hydrochloride", "labeler_name": "VERITYRX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clindamycin Hydrochloride", "active_ingredients": [{"name": "CLINDAMYCIN HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA065442", "marketing_category": "ANDA", "marketing_start_date": "20090826", "listing_expiration_date": "20261231"}