Home NDC 25021-149 Vancomycin Hydrochloride
Product NDC 25021-149
11-digit product format 250210149
Labeler code 25021
Product ID 25021-149_a05d9267-0d03-44f5-ae26-e7a523b5b862
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Vancomycin Hydrochloride
Dosage form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route INTRAVENOUS
Labeler Sagent Pharmaceuticals
Application ANDA218140
Marketing category ANDA
Marketing start 2025-06-01
Substance VANCOMYCIN HYDROCHLORIDE
Active strength 1.5 g/30mL
Pharmacologic classes Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A218140-001 VANCOMYCIN HYDROCHLORIDE VANCOMYCIN HYDROCHLORIDE EQ 750MG BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 A218140-002 VANCOMYCIN HYDROCHLORIDE VANCOMYCIN HYDROCHLORIDE EQ 1.25GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 A218140-003 VANCOMYCIN HYDROCHLORIDE VANCOMYCIN HYDROCHLORIDE EQ 1.5GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 3 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-02-19 14:30 UTC 2026-02 A218140-001 VANCOMYCIN HYDROCHLORIDE EQ 750MG BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A218140-002 VANCOMYCIN HYDROCHLORIDE EQ 1.25GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A218140-003 VANCOMYCIN HYDROCHLORIDE EQ 1.5GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A218140-001 VANCOMYCIN HYDROCHLORIDE EQ 750MG BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A218140-002 VANCOMYCIN HYDROCHLORIDE EQ 1.25GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A218140-003 VANCOMYCIN HYDROCHLORIDE EQ 1.5GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A218140-001 VANCOMYCIN HYDROCHLORIDE EQ 750MG BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A218140-002 VANCOMYCIN HYDROCHLORIDE EQ 1.25GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A218140-003 VANCOMYCIN HYDROCHLORIDE EQ 1.5GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 6a471c1ec25d…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218140-001 VANCOMYCIN HYDROCHLORIDE EQ 750MG BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218140-002 VANCOMYCIN HYDROCHLORIDE EQ 1.25GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218140-003 VANCOMYCIN HYDROCHLORIDE EQ 1.5GM BASE/VIAL POWDER / INTRAVENOUS AP 2025-03-21 a50c72e98297…
Observed Orange Book normalized TE history# openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 3 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Vancomycin Hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VANCOMYCIN HYDROCHLORIDE 1.5 g/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 71WO621TJD Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1807518 Internal RxNorm lookup 2049888 Internal RxNorm lookup 2049890 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 25021-149-30 Vancomycin Hydrochloride 30 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 30 1 25021-149-30 Vancomycin Hydrochloride 10 in 1 CARTON INJECTION, POWDER, LYOPHILIZED, 10 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 25021-149-30 25021014930 10 VIAL in 1 CARTON (25021-149-30) / 30 mL in 1 VIAL 10 vial 2025-06-01 No No Current