Ribavirin
- Product NDC
- 68382-128
- 11-digit product format
- 683820128
- Labeler code
- 68382
- Product ID
- 68382-128_731a7612-d6ab-4a9c-9347-d3e16fcfbefb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ribavirin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA077094
- Marketing category
- ANDA
- Marketing start
- 2005-12-05
- Marketing end
- 0000-00-00
- Substance
- RIBAVIRIN
- Active strength
- 500 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-128-07 | 68382012807 | 56 TABLET, FILM COATED in 1 BOTTLE (68382-128-07) | 2005-12-05 | 0000-00-00 | No | No | Current |
| 68382-128-14 | 68382012814 | 60 TABLET, FILM COATED in 1 BOTTLE (68382-128-14) | 2005-12-05 | 0000-00-00 | No | No | Current |
| 68382-128-17 | 68382012817 | 28 TABLET, FILM COATED in 1 BOTTLE (68382-128-17) | 2005-12-05 | 0000-00-00 | No | No | Current |