ondansetron hydrochloride
- Product NDC
- 63629-6709
- 11-digit product format
- 636296709
- Labeler code
- 63629
- Product ID
- 63629-6709_ae17f0b5-cec3-45f1-b1aa-ce02982d609f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ondansetron hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077050
- Marketing category
- ANDA
- Marketing start
- 2007-06-25
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6709-1 | 63629670901 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-6709-1) | 2015-08-28 | 0000-00-00 | No | No | Current |
| 63629-6709-2 | 63629670902 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-6709-2) | 2015-08-28 | 0000-00-00 | No | No | Current |
| 63629-6709-3 | 63629670903 | 15 TABLET, FILM COATED in 1 BOTTLE (63629-6709-3) | 2015-08-28 | 0000-00-00 | No | No | Current |
| 63629-6709-4 | 63629670904 | 12 TABLET, FILM COATED in 1 BOTTLE (63629-6709-4) | 2015-08-28 | 0000-00-00 | No | No | Current |