Fluocinonide
- Product NDC
- 16714-502
- 11-digit product format
- 167140502
- Labeler code
- 16714
- Product ID
- 16714-502_397ece59-0740-4980-8953-0003b8b35c70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluocinonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- NORTHSTAR RX LLC
- Application
- ANDA075008
- Marketing category
- ANDA
- Marketing start
- 1999-06-30
- Marketing end
- 0000-00-00
- Substance
- FLUOCINONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 16714-502-01 | 16714050201 | 1 TUBE in 1 CARTON (16714-502-01) > 15 g in 1 TUBE | 1 tube | 2016-08-15 | 0000-00-00 | No | No | Current |
| 16714-502-02 | 16714050202 | 1 TUBE in 1 CARTON (16714-502-02) > 30 g in 1 TUBE | 1 tube | 2016-08-15 | 0000-00-00 | No | No | Current |
| 16714-502-03 | 16714050203 | 1 TUBE in 1 CARTON (16714-502-03) > 60 g in 1 TUBE | 1 tube | 2016-08-15 | 0000-00-00 | No | No | Current |