SUGAMMADEX SODIUM
TAMARANG · SUGAMMADEX SODIUM
Open FDA's page for this record- Application number
- ANDA215260
- Sponsor name
- TAMARANG
- Submissions
- Submission type
- SUPPL
- Submission number
- 1
- Submission status
- TA
- Submission status date
- 20210917
- Review priority
- UNKNOWN
- Submission class code
- UNKNOWN
- Submission type
- ORIG
- Submission number
- 1
- Submission status
- AP
- Submission status date
- 20260728
- Review priority
- STANDARD
- Submission class code
- UNKNOWN
- Products
- Product number
- 002
- Reference drug
- No
- Brand name
- SUGAMMADEX SODIUM
- Reference standard
- No
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Marketing status
- Prescription
- Te code
- AP
- Active ingredients
- Name
- SUGAMMADEX SODIUM
- Strength
- EQ 500MG BASE/5ML (EQ 100MG BASE/ML)
- Product number
- 001
- Reference drug
- No
- Brand name
- SUGAMMADEX SODIUM
- Reference standard
- No
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Marketing status
- Prescription
- Te code
- AP
- Active ingredients
- Name
- SUGAMMADEX SODIUM
- Strength
- EQ 200MG BASE/2ML (EQ 100MG BASE/ML)
- Harmonized identifiers (openFDA)
- Application number
- ANDA215260
- Brand name
- SUGAMMADEX
- Generic name
- SUGAMMADEX SODIUM, SUGAMMADEX
- Manufacturer name
- Solupharm Pharmazeutische Erzeugnisse GmbH, Somerset Therapeutics, LLC
- Product NDC
- 55579-892, 70069-892, 70069-893
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- INTRAVENOUS
- Substance name
- SUGAMMADEX SODIUM
- RxCUI
- 1726992, 1727000
- SPL ID
- 597924ed-d1ff-91b8-e063-6294a90a353f, 6a17af4d-54a4-4366-bb3c-268afd742d0f
- SPL set ID
- f92c4e53-13d1-46f2-acf8-6730c3cfac69, 70c00636-d4ba-4939-802c-9d5a92435c93
- Package NDC
- 55579-892-01, 55579-892-10, 70069-892-01, 70069-892-10, 70069-893-01, 70069-893-10
- UNII
- ERJ6X2MXV7