Bretylium Tosylate
- Product NDC
- 61916-135
- 11-digit product format
- 619160135
- Labeler code
- 61916
- Product ID
- 61916-135_33f1cc11-9657-41b9-b604-6fa2b41e6992
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bretylium Tosylate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Pharmaceutics International, Inc. (Pii)
- Application
- ANDA204386
- Marketing category
- ANDA
- Marketing start
- 2019-06-30
- Marketing end
- 0000-00-00
- Substance
- BRETYLIUM TOSYLATE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record