DIPYRIDAMOLE
- Product NDC
- 71205-895
- 11-digit product format
- 712050895
- Labeler code
- 71205
- Product ID
- 71205-895_d384cafa-d9d7-40b1-a28a-9ac428a3ad51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIPYRIDAMOLE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040733
- Marketing category
- ANDA
- Marketing start
- 2007-02-13
- Marketing end
- 0000-00-00
- Substance
- DIPYRIDAMOLE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Decreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-895 | DIPYRIDAMOLE TABLET, FILM COATED [PROFICIENT RX LP] | 2 | Legacy NDC | 20220413_d12e1fb4-5203-46f7-a417-367966a45dd9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-895-00 | 71205089500 | 100 TABLET, FILM COATED in 1 BOTTLE (71205-895-00) | 2021-08-02 | 0000-00-00 | No | No | Current |
| 71205-895-11 | 71205089511 | 1000 TABLET, FILM COATED in 1 BOTTLE (71205-895-11) | 2021-08-02 | 0000-00-00 | No | No | Current |
| 71205-895-30 | 71205089530 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-895-30) | 2021-08-02 | 0000-00-00 | No | No | Current |
| 71205-895-55 | 71205089555 | 500 TABLET, FILM COATED in 1 BOTTLE (71205-895-55) | 2021-08-02 | 0000-00-00 | No | No | Current |
| 71205-895-60 | 71205089560 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-895-60) | 2021-08-02 | 0000-00-00 | No | No | Current |
| 71205-895-90 | 71205089590 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-895-90) | 2021-08-02 | 0000-00-00 | No | No | Current |