Home NDC 10454-710 Myobloc
Product NDC 10454-710
11-digit product format 104540710
Labeler code 10454
Product ID 10454-710_41c1a48c-e928-1099-e063-6294a90a359f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name rimabotulinumtoxinB
Dosage form INJECTION, SOLUTION
Route INTRAMUSCULAR
Labeler Solstice Neurosciences, LLC
Application BLA103846
Marketing category BLA
Marketing start 2000-12-08
Substance RIMABOTULINUMTOXINB
Active strength 2500 [USP'U]/.5mL
Pharmacologic classes Acetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Myobloc
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RIMABOTULINUMTOXINB 2500 [USP'U]/.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0Y70779M1F Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 6 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1736640 Internal RxNorm lookup 1736642 Internal RxNorm lookup 1736645 Internal RxNorm lookup 1736646 Internal RxNorm lookup 1736647 Internal RxNorm lookup 1736648 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 10454-710-10 Myobloc 1 in 1 CARTON INJECTION, SOLUTION 1 20 10454-710-10 Myobloc 0.5 mL in 1 VIAL, SINGLE-USE INJECTION, SOLUTION 0.5 20
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded rimabotulinumtoxinB ACTIVE INGREDIENT 0Y70779M1F MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5 rimabotulinumtoxinB ACTIVE MOIETY 0Y70779M1F MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5 albumin (human) INACTIVE INGREDIENT ZIF514RVZR MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5 hydrochloric acid INACTIVE INGREDIENT QTT17582CB MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5 sodium acetyltryptophanate INACTIVE INGREDIENT 3EN9H0M2FX MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5 sodium caprylate INACTIVE INGREDIENT 9XTM81VK2B MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5 sodium chloride INACTIVE INGREDIENT 451W47IQ8X MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5 sodium succinate hexahydrate INACTIVE INGREDIENT U16QOD6C4E MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10454-710 MYOBLOC (RIMABOTULINUMTOXINB) INJECTION, SOLUTION [SOLSTICE NEUROSCIENCES, LLC] 17 Current NDC, Legacy NDC, 2 package rows 20241013_675cb354-9d13-482e-8ac2-22f709c58b4f.zip
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 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Myobloc RIMABOTULINUMTOXINB Solstice Neurosciences, LLC 675cb354-9d13-482e-8ac2-22f709c58b4f 2025-10-22 Boxed warning, Warnings, Adverse reactions Exact identifier application number: BLA103846 ndc (product): 10454-710
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 103846 Myobloc rimabotulinumtoxinB 351(a) Rx 2026-07-01
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 10454-710-10 10454071010 1 VIAL, SINGLE-USE in 1 CARTON (10454-710-10) / .5 mL in 1 VIAL, SINGLE-USE 2020-01-01 0000-00-00 No No Current