Prednisone D/P
- Product NDC
- 72189-673
- 11-digit product format
- 721890673
- Labeler code
- 72189
- Product ID
- 72189-673_4f0a3946-025d-798a-e063-6294a90a831b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone D/P
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2026-04-09
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Prednisone D/P
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PREDNISONE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VB0R961HZT |
| Rxcui | 312617, 763181 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-673-21 | Prednisone D/P | 21 in 1 BLISTER PACK | TABLET | 21 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-673-21 | 72189067321 | 21 TABLET in 1 BLISTER PACK (72189-673-21) | 21 tablet | 2026-04-09 | No | No | Current |