Biifenac 500
- Product NDC
- 73516-605
- 11-digit product format
- 735160605
- Labeler code
- 73516
- Product ID
- 73516-605_284b0ef6-a630-43b4-a5a8-740f8d2b9257
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium and MENTHOL, UNSPECIFIED FORM
- Dosage form
- KIT
- Labeler
- Ashoka Health
- Application
- ANDA204132
- Marketing category
- ANDA
- Marketing start
- 2020-02-10
- Marketing end
- 0000-00-00
- Active strength
- 0
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73516-605-01 | 73516060501 | 1 KIT in 1 CARTON (73516-605-01) * 150 mL in 1 BOTTLE * 90 mL in 1 BOTTLE, WITH APPLICATOR | 1 kit | 2020-02-10 | 0000-00-00 | No | No | Current |