Betamethasone Dipropionate
- Product NDC
- 50090-2091
- 11-digit product format
- 500902091
- Labeler code
- 50090
- Product ID
- 50090-2091_47ecbd06-3db4-4c09-8940-c4d6fe17c987
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078930
- Marketing category
- ANDA
- Marketing start
- 2008-09-23
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|---|---|---|---|---|
| 50090-2091-0 | 2023-01-30 | C162847 | 48780-1 | f386c649-d89f-0266-e053-dadaa90a7c1a | These highlights do not include all the information needed to use BETAMETHASONE DIPROPIONATE CREAM safely and effectively. See full prescribing information for BETAMETHASONE DIPROPIONATE CREAM. BETAMETHASONE DIPROPIONATE cream, (augmented*) for topical use Initial U.S. Approval: 1983 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-2091-0 | Betamethasone Dipropionate | 50 g in 1 TUBE | CREAM | 50 | 11 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-2091-0 | GM - Gram | 50090-2091 | 99260126-5023-4247-a144-5e1412963a89 | 1 | 2019-05-02 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-2091 | BETAMETHASONE DIPROPIONATE CREAM [A-S MEDICATION SOLUTIONS] | 11 | Legacy NDC, 1 package rows | 20200327_8d5ab47c-6df3-47e5-b31b-9332f94b84eb.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 848176 | betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) Augmented Topical Cream | PSN | 8d5ab47c-6df3-47e5-b31b-9332f94b84eb | 11 |
| 848176 | Augmented betamethasone 0.5 MG/ML Topical Cream | SCD | 8d5ab47c-6df3-47e5-b31b-9332f94b84eb | 11 |
| 848176 | augmented betamethasone 0.05 % Topical Cream | SY | 8d5ab47c-6df3-47e5-b31b-9332f94b84eb | 11 |
| 848176 | betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) Augmented Topical Cream | SY | 8d5ab47c-6df3-47e5-b31b-9332f94b84eb | 11 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50090-2091-0 | 50090209100 | 50 g in 1 TUBE (50090-2091-0) | 50 g | 2015-10-10 | 0000-00-00 | No | No | Current |