Bacitracin

Product NDC
0009-0233
Requested package NDC
0009-0233-44
11-digit product format
000090233
Labeler code
0009
Product ID
0009-0233_fca2ebff-656e-4e5a-a635-5eb55ad9a9f1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bacitracin
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAMUSCULAR
Labeler
Pharmacia & Upjohn Company LLC
Application
ANDA060733
Marketing category
ANDA
Marketing start
1948-07-29
Marketing end
2022-01-31
Substance
BACITRACIN A
Active strength
5000 [USP'U]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0009-02330009-0233-44DDiscontinued by firm2026-07-31

Source provenance: Browse the complete Orange Book source catalog.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0009-0233-01EA - Each0009-0233087bc984-e6cf-49d6-9ce4-30f9a0982e4f12012-07-24
0009-0233-03EA - Each0009-02337ea1e7ea-bf4c-4e7d-bcbd-49a6ae8d152112012-07-24
0009-0233-44EA - Each0009-02334634a996-e0da-47bb-a341-9d903a29aed312014-01-04
0009-0233-45EA - Each0009-023385a61b29-dd14-4f82-b1a8-988a7295399412014-01-04

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0009-0233-44000090233441 VIAL in 1 CARTON (0009-0233-44) > 10 mL in 1 VIAL1 vial1948-07-292022-01-31NoNoCurrent