Ribavirin
- Product NDC
- 65841-046
- 11-digit product format
- 658410046
- Labeler code
- 65841
- Product ID
- 65841-046_f293abc5-ab36-475c-bd31-b473e926edc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ribavirin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA077094
- Marketing category
- ANDA
- Marketing start
- 2005-12-05
- Marketing end
- 0000-00-00
- Substance
- RIBAVIRIN
- Active strength
- 200 mg/1
- Pharmacologic classes
- Nucleoside Analog Antiviral [EPC], Nucleoside Analog [EXT]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65841-046-03 | 65841004603 | 168 TABLET, FILM COATED in 1 BOTTLE (65841-046-03) | | 2005-12-05 | 0000-00-00 | No | No | Current |
| 65841-046-10 | 65841004610 | 1000 TABLET, FILM COATED in 1 BOTTLE (65841-046-10) | | 2005-12-05 | 0000-00-00 | No | No | Current |
| 65841-046-28 | 65841004628 | 180 TABLET, FILM COATED in 1 BOTTLE (65841-046-28) | | 2005-12-05 | 0000-00-00 | No | No | Current |
| 65841-046-77 | 65841004677 | 10 BLISTER PACK in 1 CARTON (65841-046-77) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2005-12-05 | 0000-00-00 | No | No | Current |