Phenobarbital with Belladonna Alkaloids
- Product NDC
- 63629-2050
- 11-digit product format
- 636292050
- Labeler code
- 63629
- Product ID
- 63629-2050_14a3ef8e-54a4-462d-8050-98c1fcc0efc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-04-11
- Marketing end
- 0000-00-00
- Substance
- ATROPINE SULFATE; HYOSCYAMINE SULFATE; PHENOBARBITAL; SCOPOLAMINE HYDROBROMIDE
- Active strength
- 0 mg/1; mg/1; mg/1; mg/1
- Pharmacologic classes
- Anticholinergic [EPC], Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2050-1 | 63629205001 | 100 TABLET in 1 BOTTLE (63629-2050-1) | 100 tablet | 2022-03-08 | 0000-00-00 | No | No | Current |