Betamethasone Dipropionate USP, 0.05%
- Product NDC
- 72641-004
- 11-digit product format
- 726410004
- Labeler code
- 72641
- Product ID
- 72641-004_f98445b5-e527-4aa8-b41d-06164c2a045f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate USP, 0.05%
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Tasman Pharma Inc.
- Application
- ANDA215186
- Marketing category
- ANDA
- Marketing start
- 2022-02-18
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72641-004-15 | 72641000415 | 1 TUBE in 1 CARTON (72641-004-15) > 15 g in 1 TUBE | 1 tube | 2022-02-18 | 0000-00-00 | No | No | Current |
| 72641-004-45 | 72641000445 | 1 TUBE in 1 CARTON (72641-004-45) > 45 g in 1 TUBE | 1 tube | 2022-02-18 | 0000-00-00 | No | No | Current |