Dipyridamole
- Product NDC
- 69584-183
- 11-digit product format
- 695840183
- Labeler code
- 69584
- Product ID
- 69584-183_6cf8d202-17fc-4c56-be33-4d74f6591077
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dipyridamole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Oxford Pharmaceuticals, LLC
- Application
- ANDA040542
- Marketing category
- ANDA
- Marketing start
- 2021-04-15
- Substance
- DIPYRIDAMOLE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Decreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dipyridamole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIPYRIDAMOLE | 75 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 64ALC7F90C |
| Rxcui | 197622, 309952, 309955 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69584-183-10 | Dipyridamole | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69584-183 | DIPYRIDAMOLE TABLET, FILM COATED [OXFORD PHARMACEUTICALS, LLC] | 1 | Current NDC, Legacy NDC, 1 package rows | 20210416_f7ffd78a-e93a-40f4-8193-2d6ab4dafd00.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69584-183-10 | 69584018310 | 100 TABLET, FILM COATED in 1 BOTTLE (69584-183-10) | 2021-04-15 | 0000-00-00 | No | No | Current |