Promethazine Hydrochloride
- Product NDC
- 49999-090
- 11-digit product format
- 499990090
- Labeler code
- 49999
- Product ID
- 49999-090_5454dcfc-720a-40c2-b868-35243f19d6ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA083426
- Marketing category
- ANDA
- Marketing start
- 2010-10-28
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49999-090-05 | EA - Each | 49999-090 | bb61fd6f-ca97-4920-949c-f6ab76edb72b | 1 | 2012-07-24 |
| 49999-090-10 | EA - Each | 49999-090 | ed6993b0-c7c5-43d0-bff6-a14fdfd6de7f | 1 | 2012-07-24 |
| 49999-090-12 | EA - Each | 49999-090 | 7bd36e6f-97eb-48c7-9c42-04087c5ecd4f | 1 | 2012-07-24 |
| 49999-090-15 | EA - Each | 49999-090 | e465e7e7-1297-4e7f-9cb2-0322ba2644ee | 1 | 2012-07-24 |
| 49999-090-20 | EA - Each | 49999-090 | 959a5d8e-e5af-4d1e-832f-69a4fc4c5bd1 | 1 | 2012-07-24 |
| 49999-090-30 | EA - Each | 49999-090 | 5ad8cb71-ffba-435d-a6d0-78588b28cf08 | 1 | 2012-07-24 |
| 49999-090-60 | EA - Each | 49999-090 | be8efc83-1115-4539-92e2-08d9611f9005 | 1 | 2012-07-24 |
| 49999-090-90 | EA - Each | 49999-090 | 5cf09f61-35f1-4076-bbd1-b81834de94c8 | 1 | 2012-07-24 |