Betamethasone Sodium Phosphate and Betamethasone Acetate
- Product NDC
- 40042-048
- 11-digit product format
- 400420048
- Labeler code
- 40042
- Product ID
- 40042-048_f8cfe50b-e269-47f2-8ce6-0b40511945bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Sodium Phosphate and Betamethasone Acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
- Labeler
- PharmaForce, Inc.
- Application
- ANDA090747
- Marketing category
- ANDA
- Marketing start
- 2009-07-31
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#