Clopidogrel
- Product NDC
- 70518-0471
- 11-digit product format
- 705180471
- Labeler code
- 70518
- Product ID
- 70518-0471_edb243bb-f2fb-70f8-e053-2a95a90a64da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel bisulphate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202925
- Marketing category
- ANDA
- Marketing start
- 2017-04-28
- Marketing end
- 0000-00-00
- Substance
- CLOPIDOGREL BISULFATE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0471-0 | 70518047100 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0471-0) | 2017-04-28 | 0000-00-00 | No | No | Current |
| 70518-0471-1 | 70518047101 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0471-1) | 2019-05-29 | 0000-00-00 | No | No | Current |
| 70518-0471-2 | 70518047102 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0471-2) | 2020-01-08 | 0000-00-00 | No | No | Current |