Vancomycin Hydrochloride

Product NDC
0143-9355
11-digit product format
001439355
Labeler code
0143
Product ID
0143-9355_e298d434-6e7e-4a46-9744-a098386a89d6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Vancomycin Hydrochloride
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Labeler
Hikma Pharmaceuticals USA Inc.
Application
ANDA206616
Marketing category
ANDA
Marketing start
2018-10-03
Substance
VANCOMYCIN
Active strength
750 mg/1
Pharmacologic classes
Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Vancomycin Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VANCOMYCIN750 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii6Q205EH1VU
Rxcui1807518

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
518d3e87-1791-43fd-b421-7f508923e5f1Product name420260107
8c6bdc15-c879-407f-914d-b44fce8e7bbdProduct name120240730
324cd4ef-8967-4991-91fd-3046d51874b9Product name220240118
ba2497d8-e8e9-d71b-251e-24ac323bbaa3Product name920231206
01f96903-8ada-4a91-9a58-9f8e51b7a70aProduct name120230922
e5c5573a-2fda-453b-9d65-c6185b588ecdProduct name520220613
3a86dfd0-ed28-4976-b9ec-00923fbfbdd4Product name120220308
5d603187-d384-6e74-5fc7-30310b2b3c99Product name320190717
bec007f0-8cd6-4f79-a3df-c0d94ebb2a36Product name120190614
f4fec0bc-aaaa-4c5c-aa2b-21daf18ef477Product name120160209
a0c54c75-e1f1-eb4f-25c4-be91c2fe237dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0143-9355-01Vancomycin Hydrochloride1 in 1 VIALINJECTION, POWDER, LYOPHILIZED,14
0143-9355-10Vancomycin Hydrochloride10 in 1 CARTONINJECTION, POWDER, LYOPHILIZED,104

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0143-9355-01EA - Each0143-93555d2ce172-3a6c-46b5-a04f-0179751bc0ea12019-05-02
0143-9355-10EA - Each0143-93558354e7fd-4deb-4915-8894-9ab70c2381ee12019-05-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0143-9355VANCOMYCIN HYDROCHLORIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [HIKMA PHARMACEUTICALS USA INC.]4Current NDC, Legacy NDC, 2 package rows20220304_86950e7c-0114-47e9-8891-e09e595c48c3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1807518vancomycin 750 MG InjectionPSN86950e7c-0114-47e9-8891-e09e595c48c34
1807518vancomycin 750 MG InjectionSCD86950e7c-0114-47e9-8891-e09e595c48c34
1807518vancomycin 750 MG (as vancomycin hydrochloride 769 MG) InjectionSY86950e7c-0114-47e9-8891-e09e595c48c34

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0143-9355-01001439355011 in 1 VIALHistorical
0143-9355-100014393551010 VIAL in 1 CARTON (0143-9355-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9355-01) 10 vial2018-10-030000-00-00NoNoCurrent