Deltasone
- Product NDC
- 69668-120
- 11-digit product format
- 696680120
- Labeler code
- 69668
- Product ID
- 69668-120_5d69215d-3754-782f-e053-2a91aa0a2d82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Oculus Innovative Sciences
- Application
- ANDA083677
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/20mg
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69668-120-20 | Deltasone | 20 mg in 1 BOTTLE | TABLET | 20 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69668-120 | DELTASONE (PREDNISONE) TABLET [OCULUS INNOVATIVE SCIENCES] | 2 | Legacy NDC, 1 package rows | 20171107_18bebd56-4848-32ae-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 69668-120-20 | 69668012020 | 20 mg in 1 BOTTLE | 20 mg | Historical |