Dexamethasone Sodium Phosphate
- Product NDC
- 70518-0872
- 11-digit product format
- 705180872
- Labeler code
- 70518
- Product ID
- 70518-0872_5f11c756-56a0-5c29-e053-2a91aa0a723c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXAMETHASONE SODIUM PHOSPHATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084916
- Marketing category
- ANDA
- Marketing start
- 2017-11-28
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE
- Active strength
- 4 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#