Betamethasone Dipropionate
- Product NDC
- 68071-2850
- 11-digit product format
- 680712850
- Labeler code
- 68071
- Product ID
- 68071-2850_ebca0435-7b86-edcf-e053-2995a90a7374
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076592
- Marketing category
- ANDA
- Marketing start
- 2006-09-28
- 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 Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| dde7b902-54a1-627e-12f1-9e6d244ab88c | Product name | 4 | 20250317 |
| 69b49899-11cf-4f7e-bd0a-7dc93b27311b | Product name | 3 | 20250130 |
| bbdc14c7-d940-43b5-a2f7-36c425991f3c | Product name | 1 | 20240320 |
| 0a2fcc35-464b-9ec2-a622-753662cdd48c | Product name | 3 | 20240216 |
| 6f762601-17ef-4321-8f47-77783d3c4d8b | Product name | 3 | 20231116 |
| 1dbefad7-ab34-69c3-e51a-e7148aa38f70 | Product name | 5 | 20220921 |
| 7fea2046-07a9-4bb6-9409-828ac6f1f6df | Product name | 1 | 20210201 |
| f059f1a2-0e64-4839-9a7f-42687c91a44b | Product name | 1 | 20201007 |
| 4ea9e4b5-b452-48ad-9b25-b9a4d403405d | Product name | 1 | 20160310 |
| f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6 | Product name | 2 | 20151106 |
| 4f07db9b-3707-3e2c-05b5-d7852ba808c4 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68071-2850-5 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-6444-d83d-e063-dadaa90ab31f | These highlights do not include all the information needed to use Betamethasone Dipropionate Cream USP (Augmented), 0.05% safely and effectively. See full prescribing information for Betamethasone Dipropionate Cream USP (Augmented), 0.05% . Betamethasone Dipropionate Cream USP (Augmented), 0.05% for topical use Initial U.S. Approval: 1983 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-2850-5 | Betamethasone Dipropionate | 50 g in 1 TUBE | CREAM | 50 | 1 | |
| 68071-2850-5 | Betamethasone Dipropionate | 1 in 1 CARTON | CREAM | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68071-2850 | BETAMETHASONE DIPROPIONATE CREAM [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 2 package rows | 20221027_ebca0d24-0e59-3609-e053-2a95a90aa3db.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 848176 | betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) Augmented Topical Cream | PSN | ebca0d24-0e59-3609-e053-2a95a90aa3db | 1 |
| 848176 | Augmented betamethasone 0.5 MG/ML Topical Cream | SCD | ebca0d24-0e59-3609-e053-2a95a90aa3db | 1 |
| 848176 | augmented betamethasone 0.05 % Topical Cream | SY | ebca0d24-0e59-3609-e053-2a95a90aa3db | 1 |
| 848176 | betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) Augmented Topical Cream | SY | ebca0d24-0e59-3609-e053-2a95a90aa3db | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68071-2850-5 | 68071285005 | 1 TUBE in 1 CARTON (68071-2850-5) > 50 g in 1 TUBE | 1 tube | 2022-10-24 | 0000-00-00 | No | No | Current |