Quinosone
- Product NDC
- 72835-301
- 11-digit product format
- 728350301
- Labeler code
- 72835
- Product ID
- 72835-301_26a7b544-dda3-45da-9a16-d69561ba4587
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate and Ammonium Lactate
- Dosage form
- KIT
- Labeler
- V2 Pharma, LLC
- Application
- ANDA076793
- Marketing category
- ANDA
- Marketing start
- 2019-06-03
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72835-301-02 | GM - Gram | 72835-301 | b2ebaf93-25a8-4f6f-9e6f-cd0f1fc68b16 | 1 | 2019-07-02 |