0145-0071 : Veltin Topical Gel
| NDC: | 0145-0071 |
| Labeler: | Stiefel Laboratories Inc |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Veltin |
| Dosage Form: | Topical Gel |
| Application #: | NDA050803 |
| Rev. Date: |
NDC Package Codes:
- 0145-0071-01: 10 TUBE IN 1 CARTON (0145‑0071‑01) > 2 G IN 1 TUBE (0145‑0071‑03)
- 0145-0071-02: 1 TUBE IN 1 BLISTER PACK (0145‑0071‑02) > 2 G IN 1 TUBE (0145‑0071‑03)
- 0145-0071-10: 10 BLISTER PACK IN 1 CARTON (0145‑0071‑10) > 1 TUBE IN 1 BLISTER PACK (0145‑0071‑02) > 2 G IN 1 TUBE (0145‑0071‑03)
- 0145-0071-30: 1 TUBE IN 1 CARTON (0145‑0071‑30) > 30 G IN 1 TUBE
- 0145-0071-60: 1 TUBE IN 1 CARTON (0145‑0071‑60) > 60 G IN 1 TUBE
Active Ingredients:
- Clindamycin Phosphate
- Tretinoin
Dosage Strength:
- 10 mg/g
- .25 mg/g
Pharmaceutical Classes:
- Decreased Sebaceous Gland Activity [PE]
- Lincosamide Antibacterial [EPC]
- Lincosamides [Chemical/Ingredient]
- Retinoid [EPC]
- Retinoids [Chemical/Ingredient]
Related Products:
Based on records with the same trade name.- 16110-071 Veltin Topical Gel by Aqua Pharmaceuticals
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.