Donnatal is a Oral Elixir in the Human Prescription Drug category. It is labeled and distributed by Atlantic Biologicals Corps. The primary component is Phenobarbital; Hyoscyamine Sulfate; Scopolamine Hydrobromide; Atropine Sulfate.
Product ID | 17856-0423_42d4c5a0-3af9-481f-b29e-813b66090ba1 |
NDC | 17856-0423 |
Product Type | Human Prescription Drug |
Proprietary Name | Donnatal |
Generic Name | Phenobarbital |
Dosage Form | Elixir |
Route of Administration | ORAL |
Marketing Start Date | 2009-11-01 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Atlantic Biologicals Corps |
Substance Name | PHENOBARBITAL; HYOSCYAMINE SULFATE; SCOPOLAMINE HYDROBROMIDE; ATROPINE SULFATE |
Active Ingredient Strength | 16 mg/5mL; mg/5mL; mg/5mL; mg/5mL |
Pharm Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
DEA Schedule | CIV |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2009-11-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-05-26 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-09-06 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2009-11-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-09-06 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2009-11-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-04-01 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
PHENOBARBITAL | 16.2 mg/5mL |
SPL SET ID: | 5d69ffc1-4608-4d73-ae91-838983bcf98d |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
68151-0607 | Donnatal | Donnatal |
17856-0423 | Donnatal | Donnatal |
42291-244 | Donnatal | Donnatal |
42291-245 | Donnatal | Donnatal |
42254-268 | Donnatal | Donnatal |
59212-422 | Donnatal | Donnatal |
59212-425 | Donnatal | Donnatal |
59212-423 | Donnatal | Donnatal |
65084-123 | Donnatal | Donnatal |
66213-423 | Donnatal | Donnatal |
66213-425 | Donnatal | Donnatal |
66213-422 | Donnatal | Donnatal |
66689-063 | Donnatal | Donnatal |
0121-0531 | Phenobarbital | Phenobarbital |
0143-1445 | Phenobarbital | Phenobarbital |
0143-1450 | Phenobarbital | Phenobarbital |
0143-1455 | Phenobarbital | Phenobarbital |
0143-1458 | Phenobarbital | Phenobarbital |
0143-1495 | Phenobarbital | Phenobarbital |
0143-1500 | Phenobarbital | Phenobarbital |
0463-6145 | Phenobarbital | Phenobarbital |
0463-6151 | Phenobarbital | Phenobarbital |
0463-6160 | Phenobarbital | Phenobarbital |
0463-6170 | Phenobarbital | Phenobarbital |
0603-1508 | Phenobarbital | phenobarbital |
0603-5165 | Phenobarbital | phenobarbital |
0603-5166 | Phenobarbital | phenobarbital |
0603-5167 | Phenobarbital | phenobarbital |
0603-5168 | Phenobarbital | phenobarbital |
0904-6575 | Phenobarbital | phenobarbital |
13517-107 | Phenobarbital | phenobarbital |
13517-110 | Phenobarbital | phenobarbital |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DONNATAL 71377644 0338733 Live/Registered |
A. H. ROBINS COMPANY, INC. 1936-04-25 |