Tretinoin
- Product NDC
- 70518-3223
- 11-digit product format
- 705183223
- Labeler code
- 70518
- Product ID
- 70518-3223_cbfb1067-1cb9-2da3-e053-2995a90a17d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tretinoin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211645
- Marketing category
- ANDA
- Marketing start
- 2021-09-14
- Marketing end
- 0000-00-00
- Substance
- TRETINOIN
- Active strength
- 1 mg/g
- Pharmacologic classes
- Retinoid [EPC],Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-3223-0 | 70518322300 | 1 TUBE in 1 CARTON (70518-3223-0) > 20 g in 1 TUBE | 1 tube | 2021-09-14 | 0000-00-00 | No | No | Current |