ATROPINE SULFATE
ATROPINE SULFATE INJECTION, USP 1mg/mL 1mL VIAL
Approved
Approval ID
c4c658a0-93f0-6639-e053-2a95a90abffa
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 14, 2021
Manufacturers
FDA
HF Acquisition Co LLC, DBA HealthFirst
DUNS: 045657305
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ATROPINE SULFATE
PRODUCT DETAILS
NDC Product Code51662-1509
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Effective DateJune 14, 2021
Generic NameATROPINE SULFATE
INGREDIENTS (4)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
ATROPINE SULFATEActive
Quantity: 1 mg in 1 mL
Code: 03J5ZE7KA5
Classification: ACTIB
SULFURIC ACIDInactive
Code: O40UQP6WCF
Classification: IACT