Atropine Sulfate Injection
Somerset Therapeutics, LLC · Available
Open FDA's page for this record- Update type
- Reverified
- Initial posting date
- 01/01/2012
- Package NDC
- 70069-641-25
- Generic name
- Atropine Sulfate Injection
- Contact info
- 732-554-1037
- Availability
- Available
- Update date
- 09/11/2026
- Dosage form
- Injection
- Presentation
- Atropine Sulfate, Injection, 1 mg/1 mL (NDC 70069-641-25)
- Company name
- Somerset Therapeutics, LLC
- Status
- Current
- Therapeutic category
- Anesthesia, Neurology, Pediatric
- Harmonized identifiers (openFDA)
- Application number
- ANDA215969
- Brand name
- ATROPINE SULFATE
- Generic name
- ATROPINE SULFATE
- Manufacturer name
- Somerset Therapeutics, LLC
- Product NDC
- 70069-641, 70069-631
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- INTRAVENOUS
- Substance name
- ATROPINE SULFATE
- RxCUI
- 1190795, 1666781
- SPL ID
- 7a8a5552-fe21-4d36-8396-b7c99f41b4c4
- SPL set ID
- a6fac578-c7bc-4b3c-a454-7889cc819118
- Package NDC
- 70069-631-01, 70069-631-25, 70069-641-01, 70069-641-25
- UNII
- 03J5ZE7KA5