VANIQA
- Product NDC
- 0023-4857
- 11-digit product format
- 000234857
- Labeler code
- 0023
- Product ID
- 0023-4857_a17381ee-e2b7-4b8e-8bb9-704edf68ed22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eflornithine hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Allergan, Inc.
- Application
- NDA021145
- Marketing category
- NDA
- Marketing start
- 2013-06-01
- Marketing end
- 2023-10-31
- Substance
- EFLORNITHINE HYDROCHLORIDE
- Active strength
- 139 mg/g
- Pharmacologic classes
- Antiprotozoal [EPC], Decarboxylase Inhibitor [EPC], Decarboxylase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0023-4857-45 | 00023485745 | 1 TUBE in 1 CARTON (0023-4857-45) > 45 g in 1 TUBE | 1 tube | 2013-06-01 | 0000-00-00 | No | No | Current |