GRANISETRON HYDROCHLORIDE
- Product NDC
- 64679-661
- 11-digit product format
- 646790661
- Labeler code
- 64679
- Product ID
- 64679-661_fdb5ddb3-e3b0-4be7-8b5b-b08e1a9165ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GRANISETRON HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA078564
- Marketing category
- ANDA
- Marketing start
- 2008-06-30
- Marketing end
- 0000-00-00
- Substance
- GRANISETRON HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 64679-661-01 | 64679066101 | 5 VIAL, SINGLE-USE in 1 CARTON (64679-661-01) > 1 mL in 1 VIAL, SINGLE-USE (64679-661-04) | 2008-06-30 | 0000-00-00 | No | No | Current |
| 64679-661-03 | 64679066103 | 1 VIAL, SINGLE-USE in 1 CARTON (64679-661-03) > 1 mL in 1 VIAL, SINGLE-USE (64679-661-04) | 2008-06-30 | 0000-00-00 | No | No | Current |