Tretinoin
- Product NDC
- 53002-8100
- 11-digit product format
- 530028100
- Labeler code
- 53002
- Product ID
- 53002-8100_ec9d96ce-fa68-4e01-b4c2-e020eec051de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tretinoin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- NDA020404
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1998-04-20
- Marketing end
- 0000-00-00
- Substance
- TRETINOIN
- Active strength
- 0 mg/g
- Pharmacologic classes
- Retinoid [EPC],Retinoids [CS]
- 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 |
|---|
| 53002-8100-1 | 53002810001 | 20 g in 1 TUBE (53002-8100-1) | 20 g | 2019-01-01 | 0000-00-00 | No | No | Current |