Betamethasone dipropionate
- Product NDC
- 70518-3562
- 11-digit product format
- 705183562
- Labeler code
- 70518
- Product ID
- 70518-3562_ed342e0e-7eb5-e1c0-e053-2995a90ac187
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208885
- Marketing category
- ANDA
- Marketing start
- 2022-10-27
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3562 | BETAMETHASONE DIPROPIONATE CREAM [REMEDYREPACK INC.] | 2 | Legacy NDC | 20240116_a26c974c-0733-4a19-a761-266ca9643638.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3562-0 | 70518356200 | 1 TUBE in 1 CARTON (70518-3562-0) > 15 g in 1 TUBE | 1 tube | 2022-10-27 | 0000-00-00 | No | No | Current |