Tretinoin
- Product NDC
- 0555-0808
- 11-digit product format
- 005550808
- Labeler code
- 0555
- Product ID
- 0555-0808_4d40143c-dd75-4305-b00e-737e41e5431a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tretinoin
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA077684
- Marketing category
- ANDA
- Marketing start
- 2007-06-26
- Marketing end
- 0000-00-00
- Substance
- TRETINOIN
- Active strength
- 10 mg/1
- Pharmacologic classes
- Retinoid [EPC],Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0555-0808-02 | 00555080802 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0555-0808-02) | 2007-06-26 | 0000-00-00 | No | No | Current |