bacitracin

Generic: bacitracin

Labeler: dynarex corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name bacitracin
Generic Name bacitracin
Labeler dynarex corporation
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

bacitracin 500 [USP'U]/1000mg

Manufacturer
Dynarex Corporation

Identifiers & Regulatory

Product NDC 67777-116
Product ID 67777-116_275e9fdf-28d0-498a-e063-6294a90a7eea
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M004
Listing Expiration 2026-12-31
Marketing Start 2016-09-12

Pharmacologic Class

Physiologic Effect
decreased cell wall synthesis & repair [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67777116
Hyphenated Format 67777-116

Supplemental Identifiers

RxCUI
1648110
UPC
0616784116228 0616784116310 0616784116129
UNII
58H6RWO52I
NUI
N0000008479

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 bacitracin (source: ndc)
Generic Name bacitracin (source: ndc)
Application Number M004 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 500 [USP'U]/1000mg
source: ndc
Packaging
  • 1728 BOX in 1 CASE (67777-116-10) / 144 PACKET in 1 BOX (67777-116-11) / 900 mg in 1 PACKET
  • 72 TUBE in 1 CASE (67777-116-20) / 14000 mg in 1 TUBE (67777-116-21)
  • 72 BOX in 1 CASE (67777-116-30) / 1 TUBE in 1 BOX (67777-116-31) / 28400 mg in 1 TUBE
source: ndc

Packages (3)

Ingredients (1)

bacitracin (500 [USP'U]/1000mg)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "275e9fdf-28d0-498a-e063-6294a90a7eea", "openfda": {"nui": ["N0000008479"], "upc": ["0616784116228", "0616784116310", "0616784116129"], "unii": ["58H6RWO52I"], "rxcui": ["1648110"], "spl_set_id": ["7f8752c7-6839-261d-e053-2991aa0a0c30"], "pharm_class_pe": ["Decreased Cell Wall Synthesis & Repair [PE]"], "manufacturer_name": ["Dynarex Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1728 BOX in 1 CASE (67777-116-10)  / 144 PACKET in 1 BOX (67777-116-11)  / 900 mg in 1 PACKET", "package_ndc": "67777-116-10", "marketing_start_date": "20160912"}, {"sample": false, "description": "72 TUBE in 1 CASE (67777-116-20)  / 14000 mg in 1 TUBE (67777-116-21)", "package_ndc": "67777-116-20", "marketing_start_date": "20160912"}, {"sample": false, "description": "72 BOX in 1 CASE (67777-116-30)  / 1 TUBE in 1 BOX (67777-116-31)  / 28400 mg in 1 TUBE", "package_ndc": "67777-116-30", "marketing_start_date": "20160912"}], "brand_name": "Bacitracin", "product_id": "67777-116_275e9fdf-28d0-498a-e063-6294a90a7eea", "dosage_form": "OINTMENT", "pharm_class": ["Decreased Cell Wall Synthesis & Repair [PE]"], "product_ndc": "67777-116", "generic_name": "Bacitracin", "labeler_name": "Dynarex Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bacitracin", "active_ingredients": [{"name": "BACITRACIN", "strength": "500 [USP'U]/1000mg"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160912", "listing_expiration_date": "20261231"}