PREDNISONE
- Product NDC
- 71335-1737
- 11-digit product format
- 713351737
- Labeler code
- 71335
- Product ID
- 71335-1737_bcfaa212-63fe-4140-9672-7a31aa735038
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2018-12-07
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 3 mg/1
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-1737-1 | PREDNISONE | 30 in 1 BOTTLE | TABLET | 30 | | 100 |
| 71335-1737-2 | PREDNISONE | 90 in 1 BOTTLE | TABLET | 90 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1737 | PREDNISONE TABLET [BRYANT RANCH PREPACK] | 100 | Legacy NDC, 2 package rows | 20201209_01413391-910c-482c-8514-e469a18927ce.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1737-1 | 71335173701 | 30 TABLET in 1 BOTTLE (71335-1737-1) | 30 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |
| 71335-1737-2 | 71335173702 | 90 TABLET in 1 BOTTLE (71335-1737-2) | 90 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |