CELESTONE SOLUSPAN
- Product NDC
- 70518-1879
- 11-digit product format
- 705181879
- Labeler code
- 70518
- Product ID
- 70518-1879_82c0a036-8754-5b3d-e053-2a91aa0a1815
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Acetate and Betamethasone Sodium Phosphate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
- Labeler
- REMEDYREPACK INC.
- Application
- NDA014602
- Marketing category
- NDA
- Marketing start
- 2019-02-19
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
- Active strength
- 3 mg/mL; mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record