ReadySharp Betamethasone
- Product NDC
- 53225-3665
- 11-digit product format
- 532253665
- Labeler code
- 53225
- Product ID
- 53225-3665_cdc8226e-dc56-3ad6-e053-2a95a90a7e41
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Sodium Phosphate and Betamethasone Acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
- Labeler
- Terrain Pharmaceuticals
- Application
- ANDA090747
- Marketing category
- ANDA
- Marketing start
- 2010-04-28
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53225-3665-1 | 53225366501 | 5 mL in 1 VIAL, MULTI-DOSE (53225-3665-1) | 5 ml | 2016-10-26 | 0000-00-00 | No | No | Current |