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NDC 70934-0016-15 Promethazine Hydrochloride 25 mg/1 Details
Promethazine Hydrochloride 25 mg/1
Promethazine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is PROMETHAZINE HYDROCHLORIDE.
Product Information
NDC | 70934-0016 |
---|---|
Product ID | 70934-016_e296bb79-a52c-7ae8-e053-2995a90a925e |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Promethazine Hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Promethazine Hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 25 |
Active Ingredient Units | mg/1 |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Labeler Name | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
Pharmaceutical Class | Phenothiazine [EPC], Phenothiazines [CS] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA091179 |
Listing Certified Through | n/a |
Package
NDC 70934-0016-15 (70934001615)
NDC Package Code | 70934-016-15 |
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Billing NDC | 70934001615 |
Package | 15 TABLET in 1 BOTTLE, PLASTIC (70934-016-15) |
Marketing Start Date | 2022-06-27 |
NDC Exclude Flag | N |
Pricing Information | N/A |